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Pharmacological Countermeasures for High Altitude
Sponsor: United States Army Research Institute of Environmental Medicine
Summary
The aim of this randomized, double-blind study is to determine whether erythropoietin (Procrit) and acetazolamide: 1) mitigates altitude-induced decrements in performance at moderate altitude (3,000 m) and 2) mitigates altitude-induced decrements in performance and reduce acute mountain sickness during prolonged exposure to high altitude (4,300 m; 15 days). Volunteers will complete 5 study phases: Phase 1) sea level baseline testing and a moderate altitude exposure; Phase 2) 4 week study intervention - randomly assigned to receive erythropoietin or placebo); Phase 3) 3 1/2 days of acetazolamide and a moderate altitude exposure; Phase 4) high altitude acclimatization - 15 days at Pikes Peak; and Phase 5) two week deacclimatization. Test battery include VO2peak, 3.2 km treadmill time trial, measures of gas exchange and ventilation during rest and exercise, and blood collection.
Official title: Augmentation of Medical Readiness and Physical Performance at High Altitude Using Pharmacological Countermeasures
Key Details
Gender
All
Age Range
18 Years - 40 Years
Study Type
INTERVENTIONAL
Enrollment
18
Start Date
2022-05-27
Completion Date
2025-09-30
Last Updated
2025-03-26
Healthy Volunteers
Yes
Conditions
Interventions
Acetazolamide
Carbonic Anhydrase Inhibitor
Erythropoietin
Hormone for red blood cell
Locations (1)
USARIEM
Natick, Massachusetts, United States