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Graded Exercise Hypoxia Testing

Recruiting
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
Inclusion Criteria

• Physically active (≥150 minutes of moderate physical activity per week)

Exclusion Criteria
  • 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
NameTimeMethod
PaO₂/FiO₂ Ratio30 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
NameTimeMethod

Trial Locations

Locations (2)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

St. Mary's Hospital

🇺🇸

Rochester, Minnesota, United States

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