Graded Exercise Hypoxia Testing
- Conditions
- Hypoxia
- Registration Number
- NCT06901284
- Lead Sponsor
- Mayo Clinic
- Brief Summary
The purpose of this study is to develop a single, standardized test to determine how individuals tolerate acute hypoxia in a stepwise fashion. We aim to evaluate the association between multiple factors, such as ventilatory compensation, heart rate response, acid-base changes, sex, pulmonary function, etc, which may explain why some individuals tolerate exercise in hypoxia better than others. Identifying these factors of association will inform future pharmacological and non-pharmacological attempts to combat acute hypoxic exercise.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
• Physically active (≥150 minutes of moderate physical activity per week)
- Contraindications to exercise testing
- Currently pregnant
- Musculoskeletal or metabolic disease
- Allergies to lidocaine
- Body-mass index ≤18 or ≥35 kg·m-2
- Pacemaker
- No confounding cardiorespiratory disease
- Persistent tobacco use (>15 pack years)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PaO₂/FiO₂ Ratio 30 minutes The PaO₂/FiO₂ ratio is a widely used measure of oxygenation efficiency in the lungs. It compares the arterial oxygen partial pressure (PaO₂, measured in mmHg) to the fraction of inspired oxygen (FiO₂, expressed as a decimal). The ratio provides insight into the ability of the lungs to transfer oxygen into the bloodstream. A PaO₂/FiO₂ ratio of 300-400 is considered to be mild hypoxemia. Participants are considered as poorly tolerating hypoxia if their ratio is \<400 and good at tolerating hypoxia if their ratio is \>400.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (2)
Mayo Clinic
🇺🇸Rochester, Minnesota, United States
St. Mary's Hospital
🇺🇸Rochester, Minnesota, United States