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Completed

NCT Number: NCT06499727

HighCycle Study: Effect of Acetazolamide on Acute Mountain Sickness in Women Compared to Men

Millions of people travel to high altitude for work or leisure activities and are exposed to reduced inspiratory oxygen partial pressure and hypoxemia that may lead to altitude illness, among which the most common form is acute mountain sickness (AMS). The main AMS symptoms are headache, malaise, weakness, and fatigue. Prospective studies have shown that 20-60% of newcomers at 2500-4000m develop AMS requiring them to take medications, while, at very high altitudes, AMS may progress to high altitude cerebral oedema. Whether women are more susceptible to AMS remains insufficiently understood since no prospective study controlled for sex hormones, use of hormone contraception or assessed menstrual cycle phase (MCP) at altitude. Therefore, women remain underrepresented and poorly characterized in high altitude studies. In addition, the efficacy and safety of 250 mg/day acetazolamide, the standard recommendation for AMS prevention, has never been compared between sexes, although, women have presumably higher acetazolamide plasma concentration due to lower blood volume. Given the known dose-dependent preventive but also side effects of acetazolamide and equal proportion of women and men among mountain travellers, there is an urgent need to conclusively quantify the efficacy and safety of pre-ventive acetazolamide therapy against AMS in women compared to men.

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Key information

Age range

18 year–44 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

National Center for Cardiology and Internal Medicine

Bishkek, 720040, Kyrgyzstan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy, non-smoking men and women, age 18-44 years, without any disease and need of regular medication (including oral contraceptives).
  • BMI >18 kg/m2 and <30 kg/m2
  • Born, raised and currently living at altitudes <1000 m
  • Written informed consent
  • Premenopausal women with an eumenorrheic cycle

Exclusion criteria

  • Other types of contraceptvies (contraceptives (hormonal intrauterine device, vaginal ring, subcutaneous injections or implants, among others)
  • Pregnancy or nursing
  • Anaemic (haemoglobin concentration <10g/dl)
  • Any altitude trip <4 weks before the study
  • Allergy to acetazolamide and other sulfonamides

Treatment and study plan

Acetazolamide

Drug

Administration of 1x125mg acetazolamide in the morning, 1x125mg in the evening, starting 24 hours before departure to 3600 m.

Placebo

Drug

Administration of equally looking placebo capsules in the morning and in the evening, starting 24 hours before departure to 3600 m.

Primary outcomes

  1. Acute Mountain Sickness (AMS) Incidence, LLS 2018

    Time frame: Day 1 to 3 at 3600 m

    Sex-related difference between acetazolamide and placebo group in the incidence of AMS. AMS incidence will be defined as a Lake Louise Questionnaire version 2018 score of ≥3.

Secondary outcomes

  1. Acute Mountain Sickness (AMS) Incidence, LLS 1993

    Time frame: Day 1 to 3 at 3600 m

    Sex-related difference between acetazolamide and placebo group in the incidence of AMS. AMS incidence will be defined as a Lake Louise Questionnaire version 1993 score of ≥3.

  2. Acute Mountain Sickness (AMS) Severity, LLS 2018

    Time frame: Day 1 to 3 at 3600 m

    Sex-related difference between acetazolamide and placebo group in the AMS severity assessed by the Lake Louise Questionnaire version 2018.

  3. Acute Mountain Sickness (AMS) Severity, LLS 1993

    Time frame: Day 1 to 3 at 3600 m

    Sex-related difference between acetazolamide and placebo group in the AMS severity assessed by the Lake Louise Questionnaire version 1993.

  4. Drug-related side effects

    Time frame: Day 1 to 3 at 3600 m

    Sex-related difference between acetazolamide and placebo group in the incidence and severity of medication side effects.

  5. Arterial blood gases

    Time frame: Day 2 at 760 m and day 2 at 3600 m

    Sex-related differences between acetazolamide and placebo group in the arterial blood gases (pH, PaO2, PaCO2, SaO2).

  6. Acetazolamide plasma concentration

    Time frame: Day 2 at 3600 m

    Sex-related differences between acetazolamide plasma concentration assessed by dried blood spots.

  7. Hypoxic ventilatory response

    Time frame: Day 2 at 760 m

    Sex-related difference in the hypoxic ventilatory response assessed under FiO2 of 0.115 and while cycling on a bicycle at 30% of predicted maximal work capacity.

  8. Perceived pain visualization

    Time frame: Day 1 to 3 at 3600 m

    Sex-related differences between acetazolamide and placebo group on perceived pain sensations, visualized by the SMaRT tablet app

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

  • Laboratoire des Adaptations Métaboliques à l'Exercice en conditions Physiologiques et Pathologiques
  • National Center of Cardiology and Internal Medicine named after academician M.Mirrakhimov
  • University Hospital Heidelberg

Registry information

Official study title

HighCycle Study: Effect of Acetazolamide on Acute Mountain Sickness in Women Compared to Men: A Randomized, Placebo-Controlled, Double-Blind Parallel Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 12, 2024
Registry last updated
Jan 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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