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A Trial of Acetazolamide Versus Placebo in Preventing Mountain Sickness During Rapid Ascent

Double Blind, Placebo Controlled Randomised Trial of Acetazolamide Versus Placebo in the Prevention of Acute Mountain Sickness During Rapid Ascent

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01418157
Enrollment
380
Registered
2011-08-16
Start date
2011-08-31
Completion date
2011-10-31
Last updated
2013-06-24

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

Conditions

Acute Mountain Sickness

Keywords

Acute mountain sickness, Rapid ascent, High altitude headache, Mountain Medicine Society Nepal

Brief summary

Acute mountain sickness is a common ailment in people venturing over 2500 m altitude. Pilgrims to high altitudes are at an added risk since they are unaware and they gain height faster than the recommendations. Acetazolamide is the standard treatment and prophylaxis of acute mountain sickness. There are no randomized controlled trials that have studied protective effects of Acetazolamide in rapid ascent, and there are few conflicting studies regarding this matter. This study is a randomized, double blinded, placebo controlled trial of Acetazolamide versus placebo in 380 healthy individuals travelling to Gosaikunda Lake of Nepal in rates of ascent that are faster than the recommendations. Acetazolamide 125 mg twice daily and a placebo will be randomly assigned for 3 days and participants will be assessed at 3 stations. This study will undertake to establish the role of Acetazolamide in Rapid Ascent and will be the first RCT done in this issue. The investigators hypothesize that Acetazolamide 125mg twice daily given before rapid ascent to high altitude in Nepalese pilgrims will not be superior to placebo in decreasing both the incidence and severity of acute mountain sickness.

Interventions

DRUGAcetazolamide

125 mg twice daily until 4380 meters altitude

DRUGPlacebo

Twice daily

Sponsors

University of Oxford
CollaboratorOTHER
Wellcome Trust
CollaboratorOTHER
Mountain Medicine Society of Nepal
CollaboratorOTHER
Oxford University Clinical Research Unit, Vietnam
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Nepalese national * Aged 18 to 65 * Travelling directly from Dhunche to Gosainkunda * Rapid ascent as defined by ascent within 3 days

Exclusion criteria

* Use of any drugs for the prevention of altitude sickness or headache * Current illness * Current altitude sickness (more than one mild symptom on the Lake Louise Questionnaire (LLQ), or oxygen saturation less than 75% * Known to be pregnant or cannot exclude the possibility of being pregnant, or have missed menses by over 7 days * One night within the last 30 days spent at an altitude of 4500 metres or above * Residents of altitude more than 2500m * A known drug allergy to sulfonamides. * Treatment with any of the following in the last 2 days: acetazolamide (Diamox®), steroids (dexamethasone/decadron, prednisone), theophylline or diuretics (Lasix®), ibuprofen/motrin, naprosyn/naproxen, aspirin or acetaminophen. * Any serious intracranial abnormalities such as history of brain tumours or pseudotumour cerebri * Known severe uncontrolled headache syndrome * Diagnosed renal function impairment, diabetes, cirrhosis of liver or liver dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Diagnosis of acute mountain sicknessUpon reaching an altitude of 3300m, average expected time is 1 dayA diagnosis of AMS requires a score of three or greater on the Lake Louise Acute Mountain Sickness Questionnaire with the mandatory presence of headache and at least one of the following symptoms: dizziness or light-headedness, fatigue, gastrointestinal (GI) symptoms (nausea/vomiting), or difficulty sleeping.

Secondary

MeasureTime frameDescription
Blood oxygen saturationUpon reaching an altitude of 3300m, average expected time is 1 dayPercent
Heart rateUpon reaching an altitude of 3300m, average expected time is 1 dayBeats per minute
High altitude headacheUpon reaching an altitude of 3300m, average expected time is 1 dayHigh altitude headache severity will be scored in milimeters based on patient markings on a visual analog scale. The headache score will be identified on the designated Lake Louise Questionnaire.

Countries

Nepal

Outcome results

None listed

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