Altitude Hypoxia
Conditions
Keywords
healthy participants older than 40 years, right heart function, prevention, acetazolamide
Brief summary
Randomized, placebo controlled trial evaluating efficacy of acetazolamide on right heart function at rest in lowlanders older than 40 years travelling from 760 m to 3'100 m.
Detailed description
This is a randomized, placebo-controlled, double-blind parallel trial evaluating the efficacy of preventive acetazolamide intake on right heart function at rest in lowlanders older than 40 years travelling to altitude. Participants living in the Bishkek area, Kyrgyzstan (760m), will be transferred by car within 4h to the Tuja Ashu high altitude clinic (3'100 m), and stay there for 2 days. Acetazolamide 375mg/day (or placebo), will be administered before departure at 760 m and during the stay at altitude. Outcomes will be assessed during the stay at 3'100 m. An interim analysis will be carried out when 200 participants will have completed the study and/or after the first year. The Peto's method will be used and the trial will be stopped when pre-specified futility boundaries were crossed.
Interventions
Administration of 1x125mg acetazolamide in the morning, 2x125mg in the evening, starting 24 hours before departure to 3'100m
Administration of equally looking placebo capsules in the morning and evening, starting 24 hours before departure to 3'100m
Sponsors
Study design
Eligibility
Inclusion criteria
* Healthy men and women, age 40-75 yrs, without any disease and need of medication. * Born, raised and currently living at low altitude (\<800m). * Written informed consent. * Kyrgyz ethnicity
Exclusion criteria
* Any active respiratory, cardiovascular or other disease requiring regular treatment or being otherwise relevant for tolerance of hypoxia or altitude exposure. * Any condition that may interfere with protocol compliance including current heavy smoking (\>20 cigarettes per day or \>20 pack-years with active smoking during the last 10 years), regular use of alcohol. * Allergy to acetazolamide and other sulfonamides.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference in change of pulmonary artery pressure evaluated by echocardiography from 760 m baseline measurement to measurement at 3100 m in the acetazolamide compared to the placebo group | Day 2 at 760m and 3100m | Difference in change of pulmonary artery pressure evaluated by echocardiography from 760 m baseline measurement to measurement at 3100 m between acetazolamide and placebo groups |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| cardiac output | Day 2 at 760m and 3100m | Difference in altitude-induced change of cardiac output between acetazolamide and placebo group, measured by transthoracic echocardiography |
| right heart dimensions | Day 2 at 760m and 3100m | Difference in altitude-induced change of right heart dimensions between acetazolamide and placebo group, measured by transthoracic echocardiography |
| Difference in pulmonary artery pressure evaluated by echocardiography at 3100 m in the acetazolamide compared to the placebo group | Day 2 at 3100m | Difference in pulmonary artery pressure evaluated by echocardiography at 3100 m in the acetazolamide compared to the placebo group |
| stroke volume | Day 2 at 760m and 3100m | Difference in altitude-induced change of stroke volume between acetazolamide and placebo group, measured by transthoracic echocardiography |
| volumes | Day 2 at 760m and 3100m | Difference in altitude-induced change of volumes between acetazolamide and placebo group, measured by transthoracic echocardiography |
| right heart function | Day 2 at 760m and 3100m | Difference in altitude-induced change of right heart function between acetazolamide and placebo group, measured by transthoracic echocardiography (TAPSE) |
Countries
Kyrgyzstan