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Acute Mountain SicknessSLEEP-AIDNCT01842906

Study Looking at End Expiratory Pressure for Altitude Illness Decrease (SLEEP-AID)

A study testing Theravent in people with Acute Mountain Sickness, run by Stanford University at 1 site in Nepal.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The study is examining if an over-the-counter device (Theravent) worn while sleeping can reduce acute mountain sickness upon awakening in a high altitude trekking population. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Acute Mountain Sickness
What is being tested?
Theravent
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
219 participants
Where
1 siteNepal
Study dates
Oct 2013to Oct 2014
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • ages 18-65
  • Lake Louise Score (LLS) of < 3
  • Have not taken NSAIDs, acetazolamide, or corticosteroids in the prior week
  • Have not traveled above 4200 m in the prior week.
  • First night in Pheriche or Dingboche

Who cannot join

  • Unable to read the consent form
  • Taken NSAIDs, acetazolamide, or corticosteroids in the week prior to study enrollment.
  • Hazardous medical conditions which precludes the ability to tolerate the experimental device.
  • Pregnancy or suspected pregnancy.
  • Participants who are younger than 18 years of age and more than 65.
  • Travel to or above 4200m in the preceding week.
Show all 9Show fewer
  • Diagnosis of AMS upon enrollment (LLS ≥3 with symptoms of headache)
  • Previously diagnosed obstructive sleep apnea
  • Current symptoms of nasal congestion, rhinorrhea, sinusitis, upper respiratory infection, asthma, COPD exacerbation, pneumonia, bronchitis, or other disease of the respiratory tract.

Trial locations and contacts

1 site in 1 country.

Nepal1 site
  • Nepal

    Pheriche & Dingboche, Khumbu

Other trials in Nepal

About this study

Official title: Randomized Controlled Trial for Assessment of a Novel Non-Pharmacologic Intervention for Decrease in Altitude Illness

The study is examining if an over-the-counter device (Theravent) worn while sleeping can reduce acute mountain sickness upon awakening in a high altitude trekking population.

Read the detailed description

The specific aim of this study is to evaluate if an inexpensive and disposable end-expiratory pressure device can prevent acute mountain sickness (AMS). AMS is a common disorder found in 25-75% of hikers and trekkers in N. America and Europe who expediently ascend high altitude (>8,000 ft). This environmental malady is insidious in onset and prevention is necessary not just to limit progression to severe or fatal disease, but also to limit physiologic deterioration in those who seek enjoyment or employment at high altitudes. One of the hallmarks of both healthy and sick individuals sleeping at high altitude is an oscillating pattern of respiration marked by periods of hyperventilation alternating with apnea or hypopnea. This distressing "periodic breathing" pattern leads to a feeling of suffocation, prevents restful sleep, and the hypoxic events may well worsen ensuing AMS. Prior studies have found positive end-expiratory pressure (PEEP) an effective non-pharmacologic method to prevent nocturnal desaturations and decreasing both AMS incidence and severity.

Traditionally, PEEP devices are cumbersome and expensive, and while showing promising efficacy, are limited by both cost and portability as a useful non-pharmacologic option for AMS prophylaxis. The SLEEP-AID methodology is designed to prospectively enroll participants, randomized in a double blind placebo-controlled fashion to either the intervention [Theravent (Ventus Medical) which is single use, inexpensive, and very small] or a visually identical "sham" placebo group, and gather physiologic data to accurately reflect sleep patterns of high altitude travelers and objective as well as subjective outcomes of the intervention. The benefit of this approach will be to provide definitive data in a large and diverse cross section of a real hiking population that is generalizable to the majority of tens of millions of hikers, climbers, and high altitude tourists in the United States, Europe, Asia, and South America.

Being tested
Theravent, Control
Keywords
positive end expiratory pressure, acute mountain sickness, prevention, high altitude
Medical subject headings
Altitude Sickness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TheraventDevice

    nasal EPAP device

  • ControlDevice

    Sham device without EPAP

Study groups in NCT01842906
Study groupRoleWhat they receive
TheraventExperimentalA singe use, disposable, positive end expiratory pressure device worn over the nostrils while sleeping.
Receives: Device: Theravent
ControlSham comparatorA visibly identical sham device that does not provide positive end expiratory pressure.
Receives: Device: Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of Acute Mountain Sickness

    Acute mountain sickness will be measured by Lake Louise Criteria and diagnosed as LLC > or = to 3 with presence of a headache. Study participants will be followed approximately for 10 hours, from when they go to sleep until awakening the next morning.

    Measured: Approximately 10 hours

Secondary outcomes (3)
  1. Number of Nocturnal Desaturations

    Number of nocturnal desaturations will be measured by Watch-PAT200, a wristwatch type continuous sleep cycle and pulse oximetry analyzer. Study participants will be followed approximately for 10 hours, from when they go to sleep until awakening the next morning.

    Measured: Approximately 10 hours

  2. Acute Mountain Sickness Severity

    Severity of acute mountain sickness will be evaluated by the Lake Louise Criteria (0-15 point scale) with higher scores representing more severe symptoms. Study participants will be followed approximately for 10 hours, from when they go to sleep until awakening the next morning.

    Measured: approximately 10 hours

  3. Nocturnal Awakenings

    Number of nocturnal desaturations will be measured by Watch-PAT200, a wristwatch type continuous sleep cycle and pulse oximetry analyzer. Study participants will be followed approximately for 10 hours, from when they go to sleep until awakening the next morning.

    Measured: approximately 10 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2013 (estimated)
  2. Study startOct 2013
  3. Primary completionDec 2013
  4. Study completionOct 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
219 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01842906
Sponsor's protocol ID
SLEEP-AID
Acronym
SLEEP-AID
Status last verified
Nov 2018
First submitted
22 Apr 2013
Last updated
13 Dec 2018
Data monitoring committee
Yes
Individual data sharing
No

Publications

  • Lipman GS, Kanaan NC, Phillips C, Pomeranz D, Cain P, Fontes K, Higbee B, Meyer C, Shaheen M, Wentworth S, Walsh D. Study Looking at End Expiratory Pressure for Altitude Illness Decrease (SLEEP-AID). High Alt Med Biol. 2015 Jun;16(2):154-61. doi: 10.1089/ham.2014.1110. Epub 2015 May 7.

    PubMed 25950723

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