Skip to content

Nitrous Oxide Treatment for Tinnitus

Nitrous Oxide as Treatment for Tinnitus: A Randomized Crossover Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03365011
Enrollment
40
Registered
2017-12-07
Start date
2016-10-31
Completion date
2017-07-31
Last updated
2018-12-14

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

Conditions

Tinnitus

Keywords

Nitrous Oxide

Brief summary

Tinnitus is perception of sound without the presence of an external acoustic stimulus. Approximately 50 million Americans experience chronic tinnitus and of these, 10 million have bothersome tinnitus. The tinnitus research literature suggests that NMDA receptor antagonists may prove to be useful in reducing tinnitus. Nitrous oxide, a member of the NMDA receptor antagonist class, is a widely-used general anesthetic and sedative with a proven safety profile. The investigators hypothesized that the administration of nitrous oxide, an NMDA receptor antagonist, may be effective in treatment of tinnitus. The study design was a randomized placebo-controlled crossover trial.

Detailed description

Subjective, idiopathic, non-pulsatile tinnitus (tinnitus) is perception of sound without the presence of an external acoustic stimulus. Approximately 50 million Americans experience chronic tinnitus and of these, 10 million have bothersome tinnitus. Bothersome tinnitus is associated with poorer working memory, slower processing speeds and reaction times, and deficiencies in selective attention. Currently, effective therapies for tinnitus remain limited. Examples of therapies include external sound therapy to mask the perceived sound, behavioral therapy to habituate the patient to the perceived sound, and counseling such as cognitive behavioral therapy to address the bother and impact that tinnitus has on people's lives. Surgical treatment such as nerve transection remains controversial given its lack of efficacy and adverse event profile. There are no drugs approved by the FDA for the treatment of tinnitus. Antidepressant and antianxiety medications are prescribed to patients with tinnitus with limited benefit. Nitrous oxide is an N-methyl-D-aspartate (NMDA) receptor antagonist, a class of drugs shown to have antidepressant effects. A previous trial examined the use of nitrous oxide as a treatment for major depressive disorder (MDD). Generally, NMDA receptors promote excitation at synapses throughout the auditory pathway and play diverse roles in synaptic development and auditory information processing. In the setting of chronic damage to the auditory system, overactivation of NMDA receptors leads to aberrant spontaneous neuronal firing in the cochlea and auditory brainstem structures, which can further perpetuate damage and disease in a feed-forward mechanism. Studies by Guitton et al. and Puel et al. showed that administration of NMDA receptor antagonists prior to the administration of salicylate was effective in preventing acute excitotoxic tinnitus, establishing that salicylate induces tinnitus through its action on NMDA receptors. Thus, NMDA receptors are thought to be implicated in the generation and perpetuation of several auditory diseases including tinnitus. The investigators hypothesized that the administration of nitrous oxide, an NMDA receptor antagonist, may be a therapeutic strategy in the treatment of tinnitus. The study was a randomized placebo-controlled crossover trial. Each participant attended two intervention sessions, one treatment and one placebo. Participants eligible to participate in the study were randomly assigned to receive either placebo followed by nitrous oxide or nitrous oxide followed by placebo, according to a computer-generated randomization sequence. Only the statistician and the anesthesiology team directly involved in administration of nitrous oxide and placebo had access to the group assignments. All participants and other study team members administering survey assessments remained blinded. The two intervention sessions were held at least two weeks apart and were indistinguishable in setting, setup, and monitoring in order to maintain blinding for the participants and study team members. All intervention sessions were performed at the Washington University Clinical Research Unit, a component of the Center for Applied Research Sciences.

Interventions

Nitrous oxide gaseous mixture (50% nitrous oxide and 50% oxygen) for 40 minutes duration under anesthesia supervision with monitoring according to standards set by the American Society of Anesthesiologists.

DRUGPlacebo gas for inhalation

Placebo gaseous mixture (50% nitrogen and 50% oxygen) for 40 minutes duration under anesthesia supervision with monitoring according to standards set by the American Society of Anesthesiologists.

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult men and women 18-65 years of age * Subjective, unilateral or bilateral, non-pulsatile tinnitus scoring Bothered more than a little but not a lot, Bothered a lot, or Extremely bothered on the Global Bothersome scale * Able to give informed consent * Must be able to read, write, and understand English

Exclusion criteria

* Bipolar disorder * Schizophrenia * Schizoaffective disorder * Substance abuse or dependence (except for remote substance abuse or dependence with remission at least 1 year prior to the study and except for nicotine use disorders) * Acute medical illness that may pose subject at risk during nitrous oxide administration * Active psychotic symptoms * Patients with significant pulmonary disease and/or requiring supplemental oxygen * Contraindication against the use of nitrous oxide: * Pneumothorax * Bowel obstruction * Middle ear occlusion * Elevated intracranial pressure * Chronic cobalamin and/or folate deficiency treated with folic acid or vitamin B12 * Pregnant patients * Breastfeeding women * Previous administration of NMDA-receptor antagonists (e.g., ketamine) within the last 3 months * Tinnitus related to cochlear implantation, retrocochlear lesion, Meniere's Disease, or other known anatomic lesions of the ear or temporal bone * Tinnitus related to a Workman's Compensation claim or litigation-related event that is still pending. * Any medical condition, which, in the opinion of the PI, confounds study results or places the subject at greater risk

Design outcomes

Primary

MeasureTime frameDescription
Change in Tinnitus Functional Index (TFI) ScorePre-intervention and 1 week post-interventionChange of participant-reported tinnitus symptoms 1 week after each intervention. The Tinnitus Functional Index (TFI) is a 25-question survey assessing tinnitus impact on quality of life. Participants were asked to rate on a scale from 0-10 the degree of unpleasantness, cognitive interference, sleep disturbance, auditory difficulties, interference with relaxation, and emotional distress associated with their tinnitus. Subscores are summed and scaled to a score of 0-100. A score less than 25 indicates mild problems due to tinnitus and little need for intervention, while a score between 25-50 indicates significant problems due to tinnitus with potential need for intervention. A decrease in TFI score indicates decreased bother due to tinnitus over time, a better outcome. An increase in TFI score indicates increased bother due to tinnitus over time, a worse outcome.

Secondary

MeasureTime frameDescription
Change in Global Bothersome Scale (GBS) ScorePre-intervention and 1 week post-interventionChange in participant-reported tinnitus bother after each intervention. Global Bothersome Scale (GBS) measured participant's self-assessment of tinnitus bother on a 5-point scale ranging from Not bothered, 0 to Extremely bothered, 5. A change of 0 indicates no change in tinnitus bother over time. A change of -1 indicates somewhat improved tinnitus bother, and a change of positive 1 indicates somewhat worsened tinnitus bother. A change of positive 2 indicates significantly worsened tinnitus bother.
Patients' Global Impression of Change1 week post-interventionParticipant-reported perception of change in impact of tinnitus on quality of life since receiving each intervention

Countries

United States

Participant flow

Participants by arm

ArmCount
Placebo First
Participants are randomized to receive placebo during the first session, followed by nitrous oxide during the second session.
20
Nitrous Oxide
Participants are randomized to receive nitrous oxide during the first session, followed by placebo during the second session.
20
Total40

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject12

Baseline characteristics

CharacteristicNitrous OxideTotalPlacebo First
Age, Continuous52.8 years
STANDARD_DEVIATION 11.1
52.9 years
STANDARD_DEVIATION 11.1
53.5 years
STANDARD_DEVIATION 9.4
Global Bothersome Scale
Bothered a little, but not much
0 Participants0 Participants0 Participants
Global Bothersome Scale
Bothered a lot
5 Participants12 Participants7 Participants
Global Bothersome Scale
Bothered more than a little, but not a lot
12 Participants24 Participants12 Participants
Global Bothersome Scale
Extremely bothered
3 Participants4 Participants1 Participants
Global Bothersome Scale
Not bothered
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race
Black
2 Participants3 Participants1 Participants
Race/Ethnicity, Customized
Race
Did not respond
1 Participants1 Participants0 Participants
Race/Ethnicity, Customized
Race
Other
2 Participants5 Participants3 Participants
Race/Ethnicity, Customized
Race
White
15 Participants31 Participants16 Participants
Region of Enrollment
United States
20 Participants40 Participants20 Participants
Sex: Female, Male
Female
7 Participants20 Participants13 Participants
Sex: Female, Male
Male
13 Participants20 Participants7 Participants
Tinnitus Functional Index40 units on a scale41 units on a scale42 units on a scale

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 400 / 40
other
Total, other adverse events
0 / 403 / 40
serious
Total, serious adverse events
0 / 400 / 40

Outcome results

Primary

Change in Tinnitus Functional Index (TFI) Score

Change of participant-reported tinnitus symptoms 1 week after each intervention. The Tinnitus Functional Index (TFI) is a 25-question survey assessing tinnitus impact on quality of life. Participants were asked to rate on a scale from 0-10 the degree of unpleasantness, cognitive interference, sleep disturbance, auditory difficulties, interference with relaxation, and emotional distress associated with their tinnitus. Subscores are summed and scaled to a score of 0-100. A score less than 25 indicates mild problems due to tinnitus and little need for intervention, while a score between 25-50 indicates significant problems due to tinnitus with potential need for intervention. A decrease in TFI score indicates decreased bother due to tinnitus over time, a better outcome. An increase in TFI score indicates increased bother due to tinnitus over time, a worse outcome.

Time frame: Pre-intervention and 1 week post-intervention

ArmMeasureValue (MEAN)Dispersion
PlaceboChange in Tinnitus Functional Index (TFI) Score-1.8 score on a scaleStandard Deviation 8.8
Nitrous OxideChange in Tinnitus Functional Index (TFI) Score-2.5 score on a scaleStandard Deviation 11
Secondary

Change in Global Bothersome Scale (GBS) Score

Change in participant-reported tinnitus bother after each intervention. Global Bothersome Scale (GBS) measured participant's self-assessment of tinnitus bother on a 5-point scale ranging from Not bothered, 0 to Extremely bothered, 5. A change of 0 indicates no change in tinnitus bother over time. A change of -1 indicates somewhat improved tinnitus bother, and a change of positive 1 indicates somewhat worsened tinnitus bother. A change of positive 2 indicates significantly worsened tinnitus bother.

Time frame: Pre-intervention and 1 week post-intervention

ArmMeasureGroupValue (NUMBER)
PlaceboChange in Global Bothersome Scale (GBS) ScoreSignificantly worsened, 21 participants
PlaceboChange in Global Bothersome Scale (GBS) ScoreSomewhat improved, -15 participants
PlaceboChange in Global Bothersome Scale (GBS) ScoreNo change, 028 participants
PlaceboChange in Global Bothersome Scale (GBS) ScoreSomewhat worsened, 15 participants
Nitrous OxideChange in Global Bothersome Scale (GBS) ScoreSomewhat worsened, 12 participants
Nitrous OxideChange in Global Bothersome Scale (GBS) ScoreSignificantly worsened, 20 participants
Nitrous OxideChange in Global Bothersome Scale (GBS) ScoreNo change, 034 participants
Nitrous OxideChange in Global Bothersome Scale (GBS) ScoreSomewhat improved, -12 participants
Secondary

Patients' Global Impression of Change

Participant-reported perception of change in impact of tinnitus on quality of life since receiving each intervention

Time frame: 1 week post-intervention

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
PlaceboPatients' Global Impression of ChangeBetter, definite improvement1 Participants
PlaceboPatients' Global Impression of ChangeGreat deal better, considerable improvement0 Participants
PlaceboPatients' Global Impression of ChangeAlmost the same5 Participants
PlaceboPatients' Global Impression of ChangeA little better2 Participants
PlaceboPatients' Global Impression of ChangeSomewhat better4 Participants
PlaceboPatients' Global Impression of ChangeModerately better1 Participants
PlaceboPatients' Global Impression of ChangeNo change or worsened24 Participants
Nitrous OxidePatients' Global Impression of ChangeSomewhat better0 Participants
Nitrous OxidePatients' Global Impression of ChangeBetter, definite improvement1 Participants
Nitrous OxidePatients' Global Impression of ChangeA little better2 Participants
Nitrous OxidePatients' Global Impression of ChangeGreat deal better, considerable improvement0 Participants
Nitrous OxidePatients' Global Impression of ChangeNo change or worsened20 Participants
Nitrous OxidePatients' Global Impression of ChangeModerately better4 Participants
Nitrous OxidePatients' Global Impression of ChangeAlmost the same10 Participants

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026