Effect of Intermittent Hypoxia on Ischemia-reperfusion Injury in Healthy Individuals
1 other identifier
interventional
41
1 country
1
Brief Summary
The objective of the present study is to determine whether intermittent hypoxia protects against ischemia-reperfusion injury in young and older healthy individuals. The investigators hypothesize that intermittent hypoxia will attenuate the reduction in flow-mediated dilation following ischemia-reperfusion injury.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2019
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 30, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2021
CompletedFirst Submitted
Initial submission to the registry
June 9, 2022
CompletedFirst Posted
Study publicly available on registry
June 21, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2022
CompletedDecember 7, 2022
December 1, 2022
2.6 years
June 9, 2022
December 5, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Change in endothelial-dependent vasodilation of the brachial artery will be assessed by flow-mediated dilation using an ultrasound machine
Indicator of nitric oxide-dependent endothelial function
Measured before and 15 minutes after an ischemia-reperfusion injury.
Study Arms (2)
Intermittent hypoxia
EXPERIMENTALThe intermittent hypoxia protocol will consist of three 4-minute hypoxic cycles (arterial oxygen saturation of 80%) interspersed with 4-minute normoxic cycles.
Intermittent normoxia
SHAM COMPARATORThe intermittent normoxia protocol will consist of three 4-minute normoxic cycles (compressed air) interspersed with 4-minute normoxic cycles (room air).
Interventions
The intermittent hypoxia protocol will consist of three 4-minute hypoxic cycles (arterial oxygen saturation of 80%) interspersed with 4-minute normoxic cycles.
The intermittent normoxia protocol will consist of three 4-minute normoxic cycles (compressed air) interspersed with 4-minute normoxic cycles (room air).
Eligibility Criteria
You may qualify if:
- Men and women aged 18 to 80 years old
You may not qualify if:
- Have high blood pressure (above 130/80 mmHg)
- Are smokers
- Are pregnant
- Have a history of cardiovascular disease, diabetes or lung disease
- Are taking medication affecting the cardiovascular system
- Carpal tunnel syndrome
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Unviersity of Texas at Austin
Austin, Texas, 78712, United States
Related Publications (25)
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PMID: 20689088BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Sophie Lalande
UT Austin
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
June 9, 2022
First Posted
June 21, 2022
Study Start
May 30, 2019
Primary Completion
December 30, 2021
Study Completion
July 1, 2022
Last Updated
December 7, 2022
Record last verified: 2022-12
Data Sharing
- IPD Sharing
- Will not share