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Comparison of Temazepam and Acetazolamide to Treat Difficulty Sleeping at High Altitude

Treatment of High-altitude Sleep Disturbance: A Double-blind Comparison of Temazepam Versus Acetazolamide.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01519544
Enrollment
34
Registered
2012-01-27
Start date
2012-03-31
Completion date
2015-03-31
Last updated
2015-04-23

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

Conditions

High-altitude Sleep Disturbance

Keywords

Sleep, High Altitude, High-altitude Sleep Disturbance, Acute Mountain Sickness, Difficulty Sleeping at High Altitude, Periodic Breathing, Actigraphy, Acetazolamide, Temazepam, Groningen Sleep Quality Questionnaire survey, Stanford Sleepiness Scale, Lake Louise Acute Mountain Sickness Score

Brief summary

More than 70% of visitors to high altitude suffer poor sleep. The present study seeks to answer the question: Which medication is associated with better sleep at high altitude: temazepam or acetazolamide? The investigators hypothesis is that one medication will be associated with higher subjective sleep scores than the other. The study will compare the sleep quality of 100 subjects as they take either temazepam or acetazolamide during a visit to high altitude.

Detailed description

Difficulty sleeping is very common with acute high altitude exposure. Sleep disturbances were reported by more than 70% of participants in acute mountain sickness pharmacologic treatment trials. Difficulty sleeping is one of the primary complaints of visitors to high altitude and some authors consider difficulty sleeping to be nearly universal at high altitudes. Acetazolamide, temazepam, zolpidem and zaleplon are all effective and safe in treating the acute insomnia of high altitude. No head-to-head trials have been performed to determine the best drug class for treatment of high altitude sleep disturbances. The purpose of this study is to compare temazepam and acetazolamide in the treatment of high altitude sleep disturbances. Such knowledge will benefit the hundreds of thousands of visitors to areas of high altitude throughout the world. The study will be a convenience sample of 100 trekkers in Manang, Nepal (elevation 11,500 feet). The study will only enroll trekkers who have gained more than 200 meters (650 feet) over the preceding 24 hours. Subject enrollment will take place from March 1, 2012, through May 30, 2012. One hundred subjects will be enrolled. All subjects will complete the study in Manang, Nepal. Once an individual decides to enroll in the study, they will be instructed on the risks of the study and informed consent will be obtained. Eligibility to participate will be verified. Each subject will be randomly assigned to take 125 mg of acetazolamide or 7.5 mg of temazepam by mouth immediately prior to going to bed. Each subject will only take one dose of the medication as part of the trial. Subjects will wear a pulse oximeter and an actigraph to bed. An actigraph is an accelerometer that is worn like a wrist watch. Actigraphs can sense and record movement and for this reason are often used in sleep studies to help measure sleep duration and quality. Study participants will keep a sleep log and will be asked to complete a Groningen Sleep Quality Questionnaire Survey and Lake Louise Acute Mountain Sickness questionnaire. Subjects will also complete a Stanford Sleepiness Scale every hour for eight hours. Through both objective and subjective measurement of sleep quality, this study is designed to determine which medication is associated with improved sleep at high altitude.

Interventions

Temazepam 7.5mg capsule to be taken by mouth at bedtime for one night only.

DRUGAcetazolamide

Take Acetazolamide 125mg tablet by mouth at bedtime for one night only.

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

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

Inclusion criteria

* Trekkers on the Annapurna circuit * Must be in the process of ascent (\> 200 meters over the previous 24 hours) * Must be willing to stay 2 nights in Manang, Nepal * Healthy adults, age 18-65 * Self-report of new difficulty sleeping over the previous two days

Exclusion criteria

* Recent (\< 2 weeks) high altitude exposure (higher than 11, 500 feet or 3500 meters) * Current acute illness * Moderate to Severe Acute Mountain Sickness (Lake Louise AMS score \> 4) * High Altitude Cerebral Edema * High Altitude Pulmonary Edema * Any pre-existing sleep disorders or sleep related condition including obstructive sleep apnea, morbid obesity (BMI \> 40), restless leg syndrome, etc. * Any lung disease or condition affecting the lungs, including chronic obstructive pulmonary disease, asthma, cystic fibrosis, etc. * Congestive heart failure, pulmonary hypertension, or cardiomyopathy * Current oxygen use * Kidney disease * Liver disease * Pregnancy or breast feeding * Seizure disorder or other neurologic disorder * Glaucoma * Sulfa allergy * Acetazolamide allergy * Benzodiazepine allergy * Temazepam allergy * Currently on acetazolamide * Currently taking any benzodiazepines * Current medical treatment with any of the following: antidepressants, neuroleptics, anxiolytics, H1 antihistamines, barbiturates or hypnotics (including benzodiazepines or any other sleep aids). * Major psychiatric diagnosis (depression, anxiety, schizophrenia) * Recreational drug use * Caffeine con¬sumption \> 3 cups of coffee/day * Alcohol consumption \> 1 drink/day * Mental Retardation or Developmental Disabilities * Inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Global assessment of sleep quality using a 100mm visual analog scale1 dayThe morning after taking the study medication, subjects will be asked: How would you rate last night's sleep quality? They will mark their answer on a 100mm visual analog scale with 0mm representing 'worst night of sleep ever' and 100mm representing 'best night of sleep ever'.
The Groningen Sleep Quality Questionnaire survey1 dayThe Groningen Sleep Quality Questionnaire survey includes fifteen questions that describe sleep onset, sleep quality, awakenings, sleep duration, and wake up quality. Survey is completed by the subject.

Secondary

MeasureTime frameDescription
Time in Bed1 dayThe amount of time the subject spent in bed. Recorded by the subject.
Number of Awakenings1 dayThe number of times the subject woke up from sleep. Recorded by the subject.
Number of Awakenings to Urinate1 dayNumber of time the subject woke up from sleep to use the restroom. Recorded by the subject.
Wake Time After Sleep Onset1 dayAmount of time the subject spent awake after falling asleep. Recorded by the subject.
Terminal Wakefulness1 dayThe amount of time the subject spends in bed after waking up for the last time. Reported by the subject.
Global assessment of sleep depth1 daySubjects will be asked to rate the depth of sleep on a 100mm visual analog scales.
Global assessment of drowsiness1 daySubjects will be asked to assess their daytime drowsiness on a 100mm visual analog scale.
Sleep Onset Latency1 dayThe amount of time it takes the subject to fall asleep. Reported by the subject.
Lake Louis Acute Mountain Sickness delta score1 daySubjects will be asked to fill out a Lake Louise Acute Mountain Sickness score at the beginning and end of study participation. The Lake Louise Acute Mountain Sickness score reflects on the severity of Acute Mountain Sickness being experienced by the subject. Scores consistent moderate or severe Acute Mountain Sickness will exclude subjects from participation in the study.
Mean O2 Saturation1 dayStudy subjects will wear a pulse oximeter during the night that will record their oxygen saturation.
Proportion of time in periodic breathing1 dayVisitors to high altitude experience periodic breathing (alternating periods of increased and decreased respiratory rate) as the human body adjusts to the hypoxemia of high altitude. Both temazepam and acetazolamide have been shown to improve periodic breathing. Subjects will wear pulse oximeters. Data from the pulse oximeters will be used to calculate the amount of time that subjects spend in periodic breathing.
Number of desaturation events per hour1 dayDue to the periodic breathing that occurs at high altitude, there are frequent oxygen desaturations during sleep. Subjects will wear a pulse oximeter to determine how many time they experience a decline in their oxygen saturation during the night.
Number of awakenings per hour1 daySubjects will wear an actigraph while they sleep. Actigraphs are small wristwatch-like devices that measure subtle movements while a subject is asleep. These movements are used to objectively describe awake and asleep periods.
Sleep Efficiency1 daySubjects will wear an actigraph when they sleep. Actigraphs are small wristwatch-like devices that measure the subtle movements of a subject during the night and help objectively determine awake and asleep periods. Using data from the actigraph, one may calculate what percent of the night the subject was asleep (sleep efficiency).
Stanford Sleepiness Scale scores1 dayDuring each of the eight hours after waking up, subjects will be asked to complete a Stanford Sleepiness Scale to measure how sleepy they are.
Total Sleep Duration1 dayThe total amount of time that the subject slept. Recorded by the subject.

Countries

Nepal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026