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To Characterize the Performance of the Nasal Dilator Strip in Lowering Nasal Resistance During Sleep, Promoting Nasal Route Breathing and Reducing the Signs and Symptoms of Sleep Disordered Breathing in a Group of Chronic Nocturnal Nasal Congestion Sufferers Who Report Trouble With Their Sleep.

An Exploratory Study of a Nasal Dilator Strip

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03105297
Enrollment
91
Registered
2017-04-07
Start date
2009-09-25
Completion date
2010-08-10
Last updated
2019-07-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestion, Nasal, Sleep Disordered Breathing

Keywords

Nasal dilator strip, Sleep disordered breathing

Brief summary

To characterize the performance of the nasal dilator strip in lowering nasal resistance during sleep, promoting nasal route breathing and reducing the signs and symptoms of sleep disordered breathing in a group of chronic nocturnal nasal congestion sufferers who report trouble with their sleep.

Detailed description

This study was a baseline-controlled study. This study consisted of three phases: Baseline phase, 28 days Active phase (1 month in home treatment usage period with sleep laboratory nights after 7 (Night 8) and 28 days (Night 29) of treatment) followed by a two-night cross-over Nasal resistance phase. Screened participants were evaluated for sleep disordered breathing and PSG variables with sleep laboratory nights at Baseline, after 7 and 28 days of in house use of nasal dilator strip (Night 8 and 29 of Active phase), and at Day 30 and 31 (Night 30 and 31 of Nasal resistance phase). Participants wore the Nasal dilator strip during Active phase. Participants then entered the Nasal resistance phase of the study, which consisted of two sleep laboratory nights at Day 30 and 31 (Night 30 and 31) where they were randomized to receive a sequence of either 'strip'/' no strip' or 'no strip'/'strip as per there randomization schedule.

Interventions

DEVICEPrototype nasal dilator strip

External Prototype Nasal Dilator strip. GSK prototype nasal dilator AB 2R11. All the participants used nasal dilator strip throughout the active phase of the study (Day 1 to Day 28). Followed by that all the participants used the nasal strip on Day 29 or 30 in Nasal resistance phase of the study as per their randomization sequence.

OTHERNo strip

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

This study consisted of 3 phases baseline and active phase in which participants used the nasal dilator strip followed by 2 nights cross over nasal resistance phase in which participants were randomized to receive a sequence of strip/no strip or no strip/strip.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Nostril types I and II (Inter-axial angle below 41 degrees = type I; inter-axial angle from 41 to 70 degrees = type II) * Nasal Congestion: Have chronic nocturnal nasal congestion ('always or almost always') for at least the last year. * Sleep: Reports trouble with sleep

Exclusion criteria

* Allergy/Intolerance: Known or suspected intolerance or hypersensitivity to latex. Known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds), allergy or atopic reaction to adhesive bandages or latex. * Subject has a chronic skin condition or eczema on the face or nose. * Subject has visible open sores, sunburn, irritation on the face or nose immediately prior to treatment. * Subject has severe obstructive sleep apnea/hypopnea syndrome with an AHI score \<30 events/hour at the Baseline visit. * Subject has had a diagnosis of another major sleep disorder (i.e. primary insomnia, i.e. regularly sleeping less than 6 hours per night, sleep insufficiency, i.e. sleeping \>2 hours more on non-work days as compared to work days, narcolepsy, or periodic limb movement disorder). * Subject has a non-typical sleep schedule (e.g. shift-work). * Subject plans travel involving time-zone changes during the study period. * Subject takes medication known to have a significant effect on sleep. Use of any substance with psychotropic effects or properties known to affect sleep/wake, including but not limited to: neuroleptics, morphine/opioid derivatives, sedative antihistamines, stimulants, antidepressants, clonidine, barbiturates, anxiolytics, thalidomide, hypnotics and sedatives. Use of over the counter sleep promoting agents including diphenhydramine, doxylamine, tryptophan, valerian root, kava kava, melatonin, St John's Wort and Alluna. Use of over the counter alertness aids including caffeine and guarana. * Subject currently uses any topical nasal decongestants (nasal sprays, drops, etc). Subject must have discontinued use of topical decongestants at least 7 days prior Baseline. * Subject is experiencing an acute upper respiratory tract infection at during qualification phase and at Baseline visit. * Subject abuses alcohol (regularly drinks more than 3 drinks per day) or has a recent history (within last 2 years) of substance or alcohol abuse. Regular consumption of xanthine-containing beverages (i.e. tea, coffee, or cola) comprising usually more than 5 cups or glasses per day. * Subject has a positive drug of abuse screening result. * Subject has severe, unstable disease states (e.g. myocardial infarction, congestive heart failure, diabetes, cirrhosis, cancer, epilepsy, or stroke), pain syndromes, (e.g. fibromyalgia) or any medical or surgical condition that places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study or who in the judgement of the principal investigator would not be suitable for entry into this study. * Severe nasal obstruction caused by structural abnormality that renders the subject unsuitable for the study in the opinion of the investigator, i.e. nasal polyps, severe deviated septum. * Subject is unwilling to be videotaped or recorded during the PSG studies. * Current Treatment for Sleep Disordered Breathing a) Subject currently uses devices prescribed for sleep disordered breathing including Continuous Positive Airway Pressure (CPAP), mandibular advancement devices, tongue displacement devices. b)Over-the-counter products such as chin straps, pillows, internal/external nasal dilators are acceptable provided usage is discontinued at least 28 days prior to Baseline.

Design outcomes

Primary

MeasureTime frameDescription
Nasal Resistance in Sleeping State : Nasal Resistance Phaseupto 2 daysNasal resistance of the participants with and without strip was measured in sleeping state using a nasal mask and a flow meter to obtain a trans-nasal pressure difference and nasal flow by continuous recording over the 2 nights \[on Day 30 (Visit 5) and Day 31 (Visit 6), cumulatively\], of the nasal resistance phase.
Area at Minimum Cross Sectional Area 1 (MCA1) : Baseline PhaseDay 1Minimum cross sectional area 1 (MCA1) in the first 3 cm of the nasal cavity behind the nostril (0-3 cm), considered to be the area of the nasal valve and the distance from the nares of this restriction. MCA 1 was measured with an Acoustic Rhinometer at Day 1 (baseline phase) before and after Nasal dilator strip application.
Volume at Minimum Cross-sectional Area 1 (MCA1) : Baseline PhaseDay 1Volume of the first 3 cm of the nasal cavity behind the nostril (0-3 cm2). Volume at MCA1 was measured with an Acoustic Rhinometer at Day 1 before and after Nasal dilator strip application.
Nasal Resistance by Posterior Rhinomanometry : Baseline PhaseDay 1Nasal resistance was measured on Day 1, by a modified method of posterior rhinomanometry in awake and seated position. Using posterior rhinomanometry, the transnasal pressure difference was measured between the nasopharynx and the external nares. The technique measures the difference in transnasal pressure that drives the flow of air through the nasal cavities.

Secondary

MeasureTime frameDescription
Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the snoring percent (%) present in sleep time during the participant's domiciled sleep visits. Snoring % was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the average snore sound intensity during the participant's domiciled sleep visits. Average snore sound intensity was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase
Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the peak snore sound intensity during the participant's domiciled sleep visits. Peak snore sound intensity was recorded for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the Nasal breathing route during the participant's domiciled sleep visits. Nasal breathing route was observed for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the oro-nasal breathing route during the participant's domiciled sleep visits. Oro-nasal breathing route was observed for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31TST was measured by overnight polysomnography (PSG) using a computerized system. TST was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Sleep efficiency \[SE, a polysomnography (PSG)\] was measured as the percentage of total time in bed spent in sleep. It was calculated as the sum of Stage N1, Stage N2, Stage N3, and REM sleep, divided by the total time in bed and multiplied by 100. SE gives an overall sense of how well the participant slept and was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Sleep onset latency (SOL, a PSG parameter) was measured as the duration from the time when lights were turned off (as the participants attempted to sleep) till the time participant fell asleep. Determination of sleep and awake state was based on Electroencephalography (EEG) and behavioral parameters change. SOL was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Arousal index (AI) is the number of arousals and awakenings, reported as a total number per hour of sleep. AI was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Total Score of Composite Functional Outcomes of Sleep Questionnaire (FOSQ) : Active PhaseDay 29The FOSQ was 30-item, validated psychometric instrument that assessed the impact of disorders of excessive sleepiness on functional outcomes relevant to daily behaviors and quality of life (QoL). The responses to the questionnaire were grouped according to five factors for analysis: 1) Activity Level, 2) Vigilance, 3) Intimacy and Sexual Relationships, 4) General Productivity and 5) Social Outcome. Participant used a scale of 0 to 4 to score each question of FOSQ which then grouped in above factors (where 0= I don't do this activity for other reasons, 1= Yes, extreme difficulty, 2= Yes, moderate difficulty, 3= Yes, a little difficulty, and 4= No difficulty). Total score of composite FOSQ was the sum of scores obtained on all 30 questions of the questionnaire. The possible range for the total score of composite FOSQ was from 0-120. A higher total score of composite FOSQ indicates better QoL of the participant.
Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Total NREM (N1, 2, and 3) and REM sleep were calculated as the time spent by a participant in the NREM (measured during stable sleep) and REM sleep stages. Total NREM and REM sleep was measured by overnight PSG using a computerized system for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Respiratory Effort Related Arousal (RERA) was flattening of an inspiratory portion of nasal pressure with increased respiratory effort leading to arousal. The total number of arousals per hour were calculated as RERA. RERA was measured all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Arterial oxygen saturation (SAO2) is the fraction of \[oxygen\]-saturated hemoglobin relative to total hemoglobin (unsaturated + saturated) in the blood. SAO2 in NREM and REM sleep was measured overnight by pulse oximetry with a finger probe using a computerized system. Lowest SAO2 values observed during the NREM and REM sleep were recorded for this endpoint. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31SAO2 in sleep time was measured overnight by pulse oximetry with a finger probe using a computerized system. Mean of the observed SAO2 values during entire sleep time was reported for this endpoint. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Oxygen desaturation is the drop in blood's oxygen level per hours of sleep. Average drop in oxygen level during total sleep was measured overnight by pulse oximetry with a finger probe using a computerized system. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Percent sleep time with SAO2 greater than 90% was measured overnight by pulse oximetry with a finger probe. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Percent sleep time with SAO2 less than 90% was measured overnight by pulse oximetry with a finger probe. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Apnea/Hypopnea Index (AHI) was measured as the number of events (apnea and hypopnea) per hour of sleep. AHI was measured using overnight by PSG using a computerized system. PSG was performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31Non-Rapid eye movement (NREM) sleep stage consist of 3 progressively deeper stages of sleep: N1 (transition period from being awake to falling asleep), N2 (where breathing and heart rate began to slow) and N3 (slow wave sleep where body heals and repair itself). Sleep architecture (SA) was measured by the percentage of sleep time spent by the participants in each stage (time spent in each stage to total time spent in NREM, multiplied by 100). SA was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.
Global Self Assessment Score : Active PhaseDay 29On Day 29, prior to sleep, participants were asked to rate their overall experience with the strip as compared to before they enrolled in the study: ease of breathing, staying asleep, falling back to sleep, waking up too early, number of awakenings, falling asleep, sleep quality, sleep depth, dry mouth upon awakening, morning headache, nocturia (waking up to urinate), feeling refreshed in the morning. Experience was rated on scale of -2 to 2 were: -2 = Much worse, -1 = Somewhat worse, 0 = No change, 1 = Somewhat improve, 2 = Much improved (higher score indicated improvement).
Total Epworth Sleepiness Scale Score (ESS) : Active PhaseDay 29Participants answered the following question How likely are you to doze off or fall asleep in the following situations, in contrast to feeling just tired? 1. Sitting and reading, 2. Watching TV, 3. Sitting, inactive in a public place (e.g. a theatre or a meeting), 4. As a passenger in a car for an hour without a break, 5. Lying down to rest in the afternoon when circumstances permit, 6. Sitting and talking to someone, 7. Sitting quietly after a lunch without alcohol, and 8. In a car, while stopped for a few minutes in the traffic. Use the following scale to choose the most appropriate number for each situation: 0 = would never doze, 1 = slight chance of dozing, 2 = moderate chance of dozing, and 3 = high chance of dozing. Total ESS was calculated as the sum of all the individual scores observed for the above mentioned situations. The possible range for total ESS was 0-24. A lower total ESS indicates better sleep.
Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseDay 1, Day 8, Day 29, Day 30 and Day 31The Investigator or designee recorded the number of snores per hour during the participant's domiciled sleep visits. Numbers of snores were recorded for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Countries

Australia

Participant flow

Recruitment details

Participants were recruited from one center in Australia.

Pre-assignment details

103 participants were screened, out of which 9 were screening failure, 3 did not want to participate. Remaining 91 participants were included in the safety population.

Participants by arm

ArmCount
All Participants
All participants to whom the study treatment was dispensed were considered evaluable for baseline characteristics
91
Total91

Withdrawals & dropouts

PeriodReasonFG000
Baseline Phase (Day 1)Other21
Nasal Resistance Phase (Day 30, 31)Adverse Event1
Nasal Resistance Phase (Day 30, 31)Withdrawal by Subject7

Baseline characteristics

CharacteristicAll Participants
Age, Continuous48.8 Years
STANDARD_DEVIATION 14.23
Race/Ethnicity, Customized
Asian
9 Participants
Race/Ethnicity, Customized
Black
2 Participants
Race/Ethnicity, Customized
Caucasian
70 Participants
Race/Ethnicity, Customized
Hispanic
1 Participants
Race/Ethnicity, Customized
Other
9 Participants
Sex: Female, Male
Female
26 Participants
Sex: Female, Male
Male
65 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 910 / 700 / 550 / 55
other
Total, other adverse events
0 / 9128 / 702 / 551 / 55
serious
Total, serious adverse events
0 / 911 / 700 / 550 / 55

Outcome results

Primary

Area at Minimum Cross Sectional Area 1 (MCA1) : Baseline Phase

Minimum cross sectional area 1 (MCA1) in the first 3 cm of the nasal cavity behind the nostril (0-3 cm), considered to be the area of the nasal valve and the distance from the nares of this restriction. MCA 1 was measured with an Acoustic Rhinometer at Day 1 (baseline phase) before and after Nasal dilator strip application.

Time frame: Day 1

Population: Safety population included all participants to whom the study treatment was dispensed. Here, N signifies participants who were evaluable for this outcome measure.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Area at Minimum Cross Sectional Area 1 (MCA1) : Baseline PhaseBefore strip application1.949 cm^2Standard Deviation 0.852
All Participants (Nasal Resistance Phase)Area at Minimum Cross Sectional Area 1 (MCA1) : Baseline PhaseAfter strip application2.535 cm^2Standard Deviation 0.8735
p-value: <0.0001t-test, 1 sided
Primary

Nasal Resistance by Posterior Rhinomanometry : Baseline Phase

Nasal resistance was measured on Day 1, by a modified method of posterior rhinomanometry in awake and seated position. Using posterior rhinomanometry, the transnasal pressure difference was measured between the nasopharynx and the external nares. The technique measures the difference in transnasal pressure that drives the flow of air through the nasal cavities.

Time frame: Day 1

Population: Safety population included all participants to whom the study treatment was dispensed. Here, N signifies participants who were evaluable for this outcome measure and number analyzed signifies participants who were evaluable for the specified categories.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Nasal Resistance by Posterior Rhinomanometry : Baseline PhaseBefore strip application4.468 cmH2O/liter/secondsStandard Deviation 4.7625
All Participants (Nasal Resistance Phase)Nasal Resistance by Posterior Rhinomanometry : Baseline PhaseAfter strip application3.251 cmH2O/liter/secondsStandard Deviation 4.1677
p-value: 0.0073t-test, 1 sided
Primary

Nasal Resistance in Sleeping State : Nasal Resistance Phase

Nasal resistance of the participants with and without strip was measured in sleeping state using a nasal mask and a flow meter to obtain a trans-nasal pressure difference and nasal flow by continuous recording over the 2 nights \[on Day 30 (Visit 5) and Day 31 (Visit 6), cumulatively\], of the nasal resistance phase.

Time frame: upto 2 days

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number of participants analyzed N signifies participants who were evaluable for this outcome measure and number analyzed signifies participants who were evaluable for the specified categories.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Nasal Resistance in Sleeping State : Nasal Resistance PhaseWithout strip (Day 30 and 31)2.658 Centimeter (cm) H2O/liter/secStandard Deviation 2.4469
All Participants (Nasal Resistance Phase)Nasal Resistance in Sleeping State : Nasal Resistance PhaseWith strip (Day 30 and 31)2.202 Centimeter (cm) H2O/liter/secStandard Deviation 2.5819
p-value: 0.0147ANCOVA
Primary

Volume at Minimum Cross-sectional Area 1 (MCA1) : Baseline Phase

Volume of the first 3 cm of the nasal cavity behind the nostril (0-3 cm2). Volume at MCA1 was measured with an Acoustic Rhinometer at Day 1 before and after Nasal dilator strip application.

Time frame: Day 1

Population: Safety population included all participants to whom the study treatment was dispensed. Here, N signifies participants who were evaluable for this outcome measure.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Volume at Minimum Cross-sectional Area 1 (MCA1) : Baseline PhaseBefore strip application4.145 cm^3Standard Deviation 1.2013
All Participants (Nasal Resistance Phase)Volume at Minimum Cross-sectional Area 1 (MCA1) : Baseline PhaseAfter strip application5.043 cm^3Standard Deviation 1.4038
p-value: <0.0001t-test, 1 sided
Secondary

Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance Phase

Apnea/Hypopnea Index (AHI) was measured as the number of events (apnea and hypopnea) per hour of sleep. AHI was measured using overnight by PSG using a computerized system. PSG was performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseDay 14.08 AHI events per hourStandard Deviation 5.499
All Participants (Nasal Resistance Phase)Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseDay 84.26 AHI events per hourStandard Deviation 5.273
All Participants (Nasal Resistance Phase)Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseDay 295.07 AHI events per hourStandard Deviation 7.371
All Participants (Nasal Resistance Phase)Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)6.57 AHI events per hourStandard Deviation 10.489
All Participants (Nasal Resistance Phase)Apnea/Hypopnea Index (AHI) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)7.11 AHI events per hourStandard Deviation 12.948
Secondary

Arousal Index (AI) : Baseline, Active and Nasal Resistance Phase

Arousal index (AI) is the number of arousals and awakenings, reported as a total number per hour of sleep. AI was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseDay 125.12 Number of arousals per hourStandard Deviation 11.308
All Participants (Nasal Resistance Phase)Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseDay 825.24 Number of arousals per hourStandard Deviation 10.979
All Participants (Nasal Resistance Phase)Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseDay 2925.97 Number of arousals per hourStandard Deviation 12.916
All Participants (Nasal Resistance Phase)Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)35.33 Number of arousals per hourStandard Deviation 17.25
All Participants (Nasal Resistance Phase)Arousal Index (AI) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)38.33 Number of arousals per hourStandard Deviation 20.908
Secondary

Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance Phase

Oxygen desaturation is the drop in blood's oxygen level per hours of sleep. Average drop in oxygen level during total sleep was measured overnight by pulse oximetry with a finger probe using a computerized system. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseDay 14.41 Percentage of oxygen desaturationStandard Deviation 10.98
All Participants (Nasal Resistance Phase)Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseDay 84.68 Percentage of oxygen desaturationStandard Deviation 11.679
All Participants (Nasal Resistance Phase)Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseDay 293.49 Percentage of oxygen desaturationStandard Deviation 1.588
All Participants (Nasal Resistance Phase)Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)2.90 Percentage of oxygen desaturationStandard Deviation 2.385
All Participants (Nasal Resistance Phase)Average Oxygen Desaturation During Sleep : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)3.33 Percentage of oxygen desaturationStandard Deviation 2.113
Secondary

Average Snore Sound Intensity : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the average snore sound intensity during the participant's domiciled sleep visits. Average snore sound intensity was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 140.67 DecibelsStandard Deviation 6.278
All Participants (Nasal Resistance Phase)Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 841.85 DecibelsStandard Deviation 6.365
All Participants (Nasal Resistance Phase)Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 2944.14 DecibelsStandard Deviation 6.73
All Participants (Nasal Resistance Phase)Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)43.10 DecibelsStandard Deviation 4.78
All Participants (Nasal Resistance Phase)Average Snore Sound Intensity : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)43.89 DecibelsStandard Deviation 4.628
Secondary

Global Self Assessment Score : Active Phase

On Day 29, prior to sleep, participants were asked to rate their overall experience with the strip as compared to before they enrolled in the study: ease of breathing, staying asleep, falling back to sleep, waking up too early, number of awakenings, falling asleep, sleep quality, sleep depth, dry mouth upon awakening, morning headache, nocturia (waking up to urinate), feeling refreshed in the morning. Experience was rated on scale of -2 to 2 were: -2 = Much worse, -1 = Somewhat worse, 0 = No change, 1 = Somewhat improve, 2 = Much improved (higher score indicated improvement).

Time frame: Day 29

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable for the specified categories.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseEase of breathing1.4 Score on a scaleStandard Deviation 0.68
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseFalling asleep0.6 Score on a scaleStandard Deviation 0.78
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseStaying asleep0.8 Score on a scaleStandard Deviation 0.76
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseNumber of awakenings0.7 Score on a scaleStandard Deviation 0.77
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseFalling back to sleep0.7 Score on a scaleStandard Deviation 0.76
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseWaking up too early0.3 Score on a scaleStandard Deviation 0.63
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseSleep depth0.7 Score on a scaleStandard Deviation 0.7
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseSleep quality0.9 Score on a scaleStandard Deviation 0.69
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseNocturia (waking up to urinate)0.3 Score on a scaleStandard Deviation 0.6
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseDry mouth upon awakening0.6 Score on a scaleStandard Deviation 0.82
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseMorning headache0.4 Score on a scaleStandard Deviation 0.67
All Participants (Nasal Resistance Phase)Global Self Assessment Score : Active PhaseFeeling refreshed in the morning0.8 Score on a scaleStandard Deviation 0.76
Secondary

Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance Phase

SAO2 in sleep time was measured overnight by pulse oximetry with a finger probe using a computerized system. Mean of the observed SAO2 values during entire sleep time was reported for this endpoint. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 195.70 Percentage of SAO2Standard Deviation 1.468
All Participants (Nasal Resistance Phase)Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 895.70 Percentage of SAO2Standard Deviation 1.598
All Participants (Nasal Resistance Phase)Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 2995.64 Percentage of SAO2Standard Deviation 1.528
All Participants (Nasal Resistance Phase)Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)96.69 Percentage of SAO2Standard Deviation 1.364
All Participants (Nasal Resistance Phase)Mean Arterial Oxygen Saturation (SAO2) During Sleep Time : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)96.71 Percentage of SAO2Standard Deviation 1.188
Secondary

Number of Snores Per Hour : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the number of snores per hour during the participant's domiciled sleep visits. Numbers of snores were recorded for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseDay 1308.18 Number of snores per hourStandard Deviation 216.829
All Participants (Nasal Resistance Phase)Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseDay 8299.58 Number of snores per hourStandard Deviation 204.598
All Participants (Nasal Resistance Phase)Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseDay 29330.30 Number of snores per hourStandard Deviation 233.635
All Participants (Nasal Resistance Phase)Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)317.76 Number of snores per hourStandard Deviation 208.098
All Participants (Nasal Resistance Phase)Number of Snores Per Hour : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)324.92 Number of snores per hourStandard Deviation 190.559
Secondary

Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the peak snore sound intensity during the participant's domiciled sleep visits. Peak snore sound intensity was recorded for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 167.84 DecibelsStandard Deviation 9.944
All Participants (Nasal Resistance Phase)Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 866.44 DecibelsStandard Deviation 8.854
All Participants (Nasal Resistance Phase)Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseDay 2969.87 DecibelsStandard Deviation 8.876
All Participants (Nasal Resistance Phase)Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)69.48 DecibelsStandard Deviation 13.525
All Participants (Nasal Resistance Phase)Peak Sore Sound Intensity : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)70.28 DecibelsStandard Deviation 11.917
Secondary

Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance Phase

Arterial oxygen saturation (SAO2) is the fraction of \[oxygen\]-saturated hemoglobin relative to total hemoglobin (unsaturated + saturated) in the blood. SAO2 in NREM and REM sleep was measured overnight by pulse oximetry with a finger probe using a computerized system. Lowest SAO2 values observed during the NREM and REM sleep were recorded for this endpoint. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseREM: Day 191.33 Percentage of SAO2Standard Deviation 3.433
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseREM: Day 891.17 Percentage of SAO2Standard Deviation 3.476
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseREM: Day 2991.34 Percentage of SAO2Standard Deviation 3.219
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseREM: Without strip (Day 29 and 30)92.30 Percentage of SAO2Standard Deviation 3.541
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseREM: With strip (Day 29 and 30)92.42 Percentage of SAO2Standard Deviation 3.494
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseNREM: Day 191.01 Percentage of SAO2Standard Deviation 3.012
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseNREM: Day 890.24 Percentage of SAO2Standard Deviation 3.684
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseNREM: Day 2990.75 Percentage of SAO2Standard Deviation 3.139
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseNREM: Without strip (Day 29 and 30)91.88 Percentage of SAO2Standard Deviation 3.386
All Participants (Nasal Resistance Phase)Percentage of Lowest Arterial Oxygen Saturation (SAO2) During Rapid Eye Movement (REM) and Non-rapid Eye Movement (REM) Sleep Stage : Baseline, Active and Nasal Resistance PhaseNREM: With strip (Day 29 and 30)91.96 Percentage of SAO2Standard Deviation 3.2
Secondary

Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the Nasal breathing route during the participant's domiciled sleep visits. Nasal breathing route was observed for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 126.38 Percentage of participantsStandard Deviation 27.322
All Participants (Nasal Resistance Phase)Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 827.78 Percentage of participantsStandard Deviation 28.2
All Participants (Nasal Resistance Phase)Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 2931.25 Percentage of participantsStandard Deviation 29.558
All Participants (Nasal Resistance Phase)Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)44.71 Percentage of participantsStandard Deviation 31.139
All Participants (Nasal Resistance Phase)Percentage of Participants With Nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)48.40 Percentage of participantsStandard Deviation 28.899
Secondary

Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the oro-nasal breathing route during the participant's domiciled sleep visits. Oro-nasal breathing route was observed for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 170.92 Percentage of participantsStandard Deviation 29.496
All Participants (Nasal Resistance Phase)Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 870.26 Percentage of participantsStandard Deviation 28.578
All Participants (Nasal Resistance Phase)Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseDay 2964.44 Percentage of participantsStandard Deviation 32.627
All Participants (Nasal Resistance Phase)Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)51.04 Percentage of participantsStandard Deviation 29.894
All Participants (Nasal Resistance Phase)Percentage of Participants With Oro-nasal Breathing Route : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)47.60 Percentage of participantsStandard Deviation 28.508
Secondary

Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance Phase

Percent sleep time with SAO2 greater than 90% was measured overnight by pulse oximetry with a finger probe. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseDay 198.59 Percentage of sleep timeStandard Deviation 3.397
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseDay 897.38 Percentage of sleep timeStandard Deviation 7.383
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseDay 2998.21 Percentage of sleep timeStandard Deviation 4.021
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)98.41 Percentage of sleep timeStandard Deviation 4.016
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Greater Than 90% : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)99.18 Percentage of sleep timeStandard Deviation 1.381
Secondary

Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance Phase

Percent sleep time with SAO2 less than 90% was measured overnight by pulse oximetry with a finger probe. Oximetry measurements were performed in all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseDay 10.66 Percentage of sleep timeStandard Deviation 2.863
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseDay 81.29 Percentage of sleep timeStandard Deviation 6.713
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseDay 290.56 Percentage of sleep timeStandard Deviation 2.742
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)0.12 Percentage of sleep timeStandard Deviation 0.475
All Participants (Nasal Resistance Phase)Percentage of Sleep Time With Arterial Oxygen Saturation (SAO2) Less Than 90% : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)0.49 Percentage of sleep timeStandard Deviation 2.533
Secondary

Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance Phase

Respiratory Effort Related Arousal (RERA) was flattening of an inspiratory portion of nasal pressure with increased respiratory effort leading to arousal. The total number of arousals per hour were calculated as RERA. RERA was measured all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseDay 114.62 RERA per hourStandard Deviation 9.006
All Participants (Nasal Resistance Phase)Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseDay 816.80 RERA per hourStandard Deviation 9.611
All Participants (Nasal Resistance Phase)Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseDay 2916.30 RERA per hourStandard Deviation 10.602
All Participants (Nasal Resistance Phase)Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)20.65 RERA per hourStandard Deviation 11.789
All Participants (Nasal Resistance Phase)Respiratory Effort Related Arousals (RERA) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)23.88 RERA per hourStandard Deviation 13.757
Secondary

Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase

Non-Rapid eye movement (NREM) sleep stage consist of 3 progressively deeper stages of sleep: N1 (transition period from being awake to falling asleep), N2 (where breathing and heart rate began to slow) and N3 (slow wave sleep where body heals and repair itself). Sleep architecture (SA) was measured by the percentage of sleep time spent by the participants in each stage (time spent in each stage to total time spent in NREM, multiplied by 100). SA was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N1: Day 18.30 Percentage of sleep timeStandard Deviation 4.123
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N1: Day 87.58 Percentage of sleep timeStandard Deviation 4.14
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N1: Day 298.46 Percentage of sleep timeStandard Deviation 5.468
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N1: Without strip (Day 29 and 30)7.65 Percentage of sleep timeStandard Deviation 6.896
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N1: With strip (Day 29 and 30)8.82 Percentage of sleep timeStandard Deviation 11.567
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N2: Day 147.93 Percentage of sleep timeStandard Deviation 6.881
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N2: Day 848.00 Percentage of sleep timeStandard Deviation 7.876
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N2: Day 2947.12 Percentage of sleep timeStandard Deviation 6.558
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N2: Without strip (Day 29 and 30)55.41 Percentage of sleep timeStandard Deviation 8.129
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N2: With strip (Day 29 and 30)54.71 Percentage of sleep timeStandard Deviation 10.212
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N3: Day 122.83 Percentage of sleep timeStandard Deviation 7.249
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N3: Day 822.14 Percentage of sleep timeStandard Deviation 7.06
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N3 at Day 2922.38 Percentage of sleep timeStandard Deviation 6.779
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N3: Without strip (Day 29 and 30)19.02 Percentage of sleep timeStandard Deviation 8.255
All Participants (Nasal Resistance Phase)Sleep Architecture (Non-Rapid Eye Movement- Stages N1, N2 and N3) : Baseline, Active and Nasal Resistance Phase% N3: With strip (Day 29 and 30)18.37 Percentage of sleep timeStandard Deviation 9.654
Secondary

Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance Phase

Sleep efficiency \[SE, a polysomnography (PSG)\] was measured as the percentage of total time in bed spent in sleep. It was calculated as the sum of Stage N1, Stage N2, Stage N3, and REM sleep, divided by the total time in bed and multiplied by 100. SE gives an overall sense of how well the participant slept and was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseDay 180.50 Percentage of sleep timeStandard Deviation 10.631
All Participants (Nasal Resistance Phase)Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseDay 881.66 Percentage of sleep timeStandard Deviation 10.184
All Participants (Nasal Resistance Phase)Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseDay 2982.25 Percentage of sleep timeStandard Deviation 11.607
All Participants (Nasal Resistance Phase)Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)75.56 Percentage of sleep timeStandard Deviation 16.095
All Participants (Nasal Resistance Phase)Sleep Efficiency (SE) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)73.63 Percentage of sleep timeStandard Deviation 19.13
Secondary

Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance Phase

Sleep onset latency (SOL, a PSG parameter) was measured as the duration from the time when lights were turned off (as the participants attempted to sleep) till the time participant fell asleep. Determination of sleep and awake state was based on Electroencephalography (EEG) and behavioral parameters change. SOL was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseDay 113.86 MinutesStandard Deviation 18.469
All Participants (Nasal Resistance Phase)Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseDay 814.92 MinutesStandard Deviation 17.275
All Participants (Nasal Resistance Phase)Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)14.29 MinutesStandard Deviation 19.943
All Participants (Nasal Resistance Phase)Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)18.45 MinutesStandard Deviation 23.937
All Participants (Nasal Resistance Phase)Sleep Onset Latency (SOL) : Baseline, Active and Nasal Resistance PhaseDay 299.69 MinutesStandard Deviation 8.877
Secondary

Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance Phase

The Investigator or designee recorded the snoring percent (%) present in sleep time during the participant's domiciled sleep visits. Snoring % was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 140.33 Percentage of sleep timeStandard Deviation 27.444
All Participants (Nasal Resistance Phase)Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 838.70 Percentage of sleep timeStandard Deviation 25.826
All Participants (Nasal Resistance Phase)Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseDay 2942.41 Percentage of sleep timeStandard Deviation 28.974
All Participants (Nasal Resistance Phase)Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)42.11 Percentage of sleep timeStandard Deviation 27.167
All Participants (Nasal Resistance Phase)Snoring Percent of Sleep Time : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)43.22 Percentage of sleep timeStandard Deviation 24.704
Secondary

Total Epworth Sleepiness Scale Score (ESS) : Active Phase

Participants answered the following question How likely are you to doze off or fall asleep in the following situations, in contrast to feeling just tired? 1. Sitting and reading, 2. Watching TV, 3. Sitting, inactive in a public place (e.g. a theatre or a meeting), 4. As a passenger in a car for an hour without a break, 5. Lying down to rest in the afternoon when circumstances permit, 6. Sitting and talking to someone, 7. Sitting quietly after a lunch without alcohol, and 8. In a car, while stopped for a few minutes in the traffic. Use the following scale to choose the most appropriate number for each situation: 0 = would never doze, 1 = slight chance of dozing, 2 = moderate chance of dozing, and 3 = high chance of dozing. Total ESS was calculated as the sum of all the individual scores observed for the above mentioned situations. The possible range for total ESS was 0-24. A lower total ESS indicates better sleep.

Time frame: Day 29

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, N signifies participants who were evaluable for this outcome measure.

ArmMeasureValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Total Epworth Sleepiness Scale Score (ESS) : Active Phase7.410 Score on scaleStandard Deviation 4.6021
Secondary

Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance Phase

Total NREM (N1, 2, and 3) and REM sleep were calculated as the time spent by a participant in the NREM (measured during stable sleep) and REM sleep stages. Total NREM and REM sleep was measured by overnight PSG using a computerized system for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseNREM: Day 1296.30 MinutesStandard Deviation 41.046
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseNREM: Day 8294.17 MinutesStandard Deviation 46.66
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseNREM: Day 29289.48 MinutesStandard Deviation 52.366
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseNREM: Without strip (Day 30 and 31)264.82 MinutesStandard Deviation 79.545
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseNREM: With strip (Day 30 and 31)249.63 MinutesStandard Deviation 81.397
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseREM: Day 173.10 MinutesStandard Deviation 20.976
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseREM: Day 877.52 MinutesStandard Deviation 22.313
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseREM: Day 2976.53 MinutesStandard Deviation 25.039
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseREM: Without strip (Day 30 and 31)52.84 MinutesStandard Deviation 23.452
All Participants (Nasal Resistance Phase)Total Non-rapid Eye Movement (NREM) and Rapid Eye Movement (REM) Sleep : Baseline, Active and Nasal Resistance PhaseREM: With strip (Day 30 and 31)55.04 MinutesStandard Deviation 28.592
Secondary

Total Score of Composite Functional Outcomes of Sleep Questionnaire (FOSQ) : Active Phase

The FOSQ was 30-item, validated psychometric instrument that assessed the impact of disorders of excessive sleepiness on functional outcomes relevant to daily behaviors and quality of life (QoL). The responses to the questionnaire were grouped according to five factors for analysis: 1) Activity Level, 2) Vigilance, 3) Intimacy and Sexual Relationships, 4) General Productivity and 5) Social Outcome. Participant used a scale of 0 to 4 to score each question of FOSQ which then grouped in above factors (where 0= I don't do this activity for other reasons, 1= Yes, extreme difficulty, 2= Yes, moderate difficulty, 3= Yes, a little difficulty, and 4= No difficulty). Total score of composite FOSQ was the sum of scores obtained on all 30 questions of the questionnaire. The possible range for the total score of composite FOSQ was from 0-120. A higher total score of composite FOSQ indicates better QoL of the participant.

Time frame: Day 29

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, N signifies participants who were evaluable for this outcome measure.

ArmMeasureValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Total Score of Composite Functional Outcomes of Sleep Questionnaire (FOSQ) : Active Phase17.55 Score on a scaleStandard Deviation 2.129
Secondary

Total Sleep Time (TST) : Baseline, Active and Nasal Resistance Phase

TST was measured by overnight polysomnography (PSG) using a computerized system. TST was measured for all participants with strip on Day 1 (Visit 2) in baseline phase, Day 8 (Visit 3) and Day 29 (Visit 4) in active phase, and in participants with and without strip on Day 30 (Visit 5) and Day 31 (Visit 6) cumulatively, in nasal resistance phase.

Time frame: Day 1, Day 8, Day 29, Day 30 and Day 31

Population: Per protocol population included all participants who fully complied with all study procedures and restrictions. Here, number analyzed signifies participants who were evaluable at specified timepoints.

ArmMeasureGroupValue (MEAN)Dispersion
All Participants (Nasal Resistance Phase)Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseDay 1369.54 MinutesStandard Deviation 52.629
All Participants (Nasal Resistance Phase)Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseDay 8371.97 MinutesStandard Deviation 58.359
All Participants (Nasal Resistance Phase)Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseDay 29366.26 MinutesStandard Deviation 69.722
All Participants (Nasal Resistance Phase)Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseWithout strip (Day 30 and 31)317.98 MinutesStandard Deviation 91.91
All Participants (Nasal Resistance Phase)Total Sleep Time (TST) : Baseline, Active and Nasal Resistance PhaseWith strip (Day 30 and 31)304.65 MinutesStandard Deviation 101.447

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026