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Effect of Short-term Simulated Altitude Exposure on Cardiopulmonary Functional Capacity

Not Applicable
Terminated
Conditions
Hypoxia
Interventions
Other: Hypoxia
Other: Normoxia
Registration Number
NCT02523716
Lead Sponsor
University of Limerick
Brief Summary

To determine if exposure of older volunteers, age 50-70y, who are healthy, but not physically active, to 7 days of mild hypoxia (15% oxygen, equivalent 2440m) will improve cardiopulmonary functional capacity.

Detailed Description

Background There is an urgent need to reduce morbidity and mortality following major surgery. Bodily demands for oxygen increase after major surgery, and postoperative outcomes can be predicted by quantifying the body's ability to meet increased mitochondrial demand for oxygen using cardiopulmonary exercise testing (CPET).

Design This is a preliminary, physiological study to establish the baseline relationship between mild hypoxia exposure and cardiopulmonary function. This study will begin to examine the feasibility and potential for achieving risk modification through low-oxygen (hypoxic) conditioning, in which a safe and convenient "dose" of mild hypoxia is used to improve CPET derived variables that predict mortality following surgery.

The study will use a randomised, double blind, sham-controlled, crossover design. After a baseline CPET test, participants will be exposed to 7 days of either mildly hypoxic or normoxic air. A follow up CPET test will then be used to determine if cardiopulmonary functional capacity increased after exposure. After a two week washout period, participants will return for a second 7-day session where the alternate exposure will be given. A final follow-up CPET test will then be performed.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
8
Inclusion Criteria
  • Healthy male and female individuals aged 50-70 years with sedentary lifestyles.
Exclusion Criteria
  • Known intolerance to altitude identified by the participant's clinical examination, history and pre-altitude screening completed by the research clinician.
  • Non-availability and/or suitability to complete the required residential period within the altitude centre.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
HypoxiaHypoxiaMild hypoxia of 15% oxygen, equivalent altitude of 2440m over a period of 7 days
NormoxiaNormoxiaExposure to normal, sea-level air
Primary Outcome Measures
NameTimeMethod
Change in Cardio pulmonary functional variablesChange in Cardio pulmonary functional variables between day 0 and day 7 in each arm of the study.

Assess cardio pulmonary functional variables using cardio pulmonary exercise testing (CPET) prior and following participants completing each arm of the study

Secondary Outcome Measures
NameTimeMethod
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