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

Primary Purpose

High-altitude Sleep Disturbance

Status
Completed
Phase
Not Applicable
Locations
Nepal
Study Type
Interventional
Intervention
Temazepam
Acetazolamide
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for High-altitude Sleep Disturbance focused on measuring 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

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Himalayan Rescue Location clinic in Manang

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Temazepam

Acetazolamide

Arm Description

50 subjects are instructed to take 7.5mg temazepam by mouth prior to going to sleep for one night only.

50 subjects are instructed to take 125mg of acetazolamide by mouth prior to going to sleep one night only.

Outcomes

Primary Outcome Measures

Global assessment of sleep quality using a 100mm visual analog scale
The 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 survey
The 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 Outcome Measures

Sleep Onset Latency
The amount of time it takes the subject to fall asleep. Reported by the subject.
Total Sleep Duration
The total amount of time that the subject slept. Recorded by the subject.
Time in Bed
The amount of time the subject spent in bed. Recorded by the subject.
Number of Awakenings
The number of times the subject woke up from sleep. Recorded by the subject.
Number of Awakenings to Urinate
Number of time the subject woke up from sleep to use the restroom. Recorded by the subject.
Wake Time After Sleep Onset
Amount of time the subject spent awake after falling asleep. Recorded by the subject.
Terminal Wakefulness
The amount of time the subject spends in bed after waking up for the last time. Reported by the subject.
Global assessment of sleep depth
Subjects will be asked to rate the depth of sleep on a 100mm visual analog scales.
Global assessment of drowsiness
Subjects will be asked to assess their daytime drowsiness on a 100mm visual analog scale.
Stanford Sleepiness Scale scores
During each of the eight hours after waking up, subjects will be asked to complete a Stanford Sleepiness Scale to measure how sleepy they are.
Lake Louis Acute Mountain Sickness delta score
Subjects 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 Saturation
Study subjects will wear a pulse oximeter during the night that will record their oxygen saturation.
Proportion of time in periodic breathing
Visitors 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 hour
Due 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 hour
Subjects 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 Efficiency
Subjects 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).

Full Information

First Posted
January 24, 2012
Last Updated
April 22, 2015
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01519544
Brief Title
Comparison of Temazepam and Acetazolamide to Treat Difficulty Sleeping at High Altitude
Official Title
Treatment of High-altitude Sleep Disturbance: A Double-blind Comparison of Temazepam Versus Acetazolamide.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Temazepam
Arm Type
Active Comparator
Arm Description
50 subjects are instructed to take 7.5mg temazepam by mouth prior to going to sleep for one night only.
Arm Title
Acetazolamide
Arm Type
Active Comparator
Arm Description
50 subjects are instructed to take 125mg of acetazolamide by mouth prior to going to sleep one night only.
Intervention Type
Drug
Intervention Name(s)
Temazepam
Other Intervention Name(s)
Restoril
Intervention Description
Temazepam 7.5mg capsule to be taken by mouth at bedtime for one night only.
Intervention Type
Drug
Intervention Name(s)
Acetazolamide
Other Intervention Name(s)
Diamox
Intervention Description
Take Acetazolamide 125mg tablet by mouth at bedtime for one night only.
Primary Outcome Measure Information:
Title
Global assessment of sleep quality using a 100mm visual analog scale
Description
The 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'.
Time Frame
1 day
Title
The Groningen Sleep Quality Questionnaire survey
Description
The 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.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Sleep Onset Latency
Description
The amount of time it takes the subject to fall asleep. Reported by the subject.
Time Frame
1 day
Title
Total Sleep Duration
Description
The total amount of time that the subject slept. Recorded by the subject.
Time Frame
1 day
Title
Time in Bed
Description
The amount of time the subject spent in bed. Recorded by the subject.
Time Frame
1 day
Title
Number of Awakenings
Description
The number of times the subject woke up from sleep. Recorded by the subject.
Time Frame
1 day
Title
Number of Awakenings to Urinate
Description
Number of time the subject woke up from sleep to use the restroom. Recorded by the subject.
Time Frame
1 day
Title
Wake Time After Sleep Onset
Description
Amount of time the subject spent awake after falling asleep. Recorded by the subject.
Time Frame
1 day
Title
Terminal Wakefulness
Description
The amount of time the subject spends in bed after waking up for the last time. Reported by the subject.
Time Frame
1 day
Title
Global assessment of sleep depth
Description
Subjects will be asked to rate the depth of sleep on a 100mm visual analog scales.
Time Frame
1 day
Title
Global assessment of drowsiness
Description
Subjects will be asked to assess their daytime drowsiness on a 100mm visual analog scale.
Time Frame
1 day
Title
Stanford Sleepiness Scale scores
Description
During each of the eight hours after waking up, subjects will be asked to complete a Stanford Sleepiness Scale to measure how sleepy they are.
Time Frame
1 day
Title
Lake Louis Acute Mountain Sickness delta score
Description
Subjects 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.
Time Frame
1 day
Title
Mean O2 Saturation
Description
Study subjects will wear a pulse oximeter during the night that will record their oxygen saturation.
Time Frame
1 day
Title
Proportion of time in periodic breathing
Description
Visitors 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.
Time Frame
1 day
Title
Number of desaturation events per hour
Description
Due 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.
Time Frame
1 day
Title
Number of awakenings per hour
Description
Subjects 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.
Time Frame
1 day
Title
Sleep Efficiency
Description
Subjects 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).
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norman S Harris, MD, MFA
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Himalayan Rescue Location clinic in Manang
City
Manang
State/Province
District of Manang
ZIP/Postal Code
33500
Country
Nepal

12. IPD Sharing Statement

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

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