NCT05423470

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2019

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 30, 2019

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2021

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 9, 2022

Completed
12 days until next milestone

First Posted

Study publicly available on registry

June 21, 2022

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2022

Completed
Last Updated

December 7, 2022

Status Verified

December 1, 2022

Enrollment Period

2.6 years

First QC Date

June 9, 2022

Last Update Submit

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

EXPERIMENTAL

The intermittent hypoxia protocol will consist of three 4-minute hypoxic cycles (arterial oxygen saturation of 80%) interspersed with 4-minute normoxic cycles.

Behavioral: Intermittent hypoxia

Intermittent normoxia

SHAM COMPARATOR

The intermittent normoxia protocol will consist of three 4-minute normoxic cycles (compressed air) interspersed with 4-minute normoxic cycles (room air).

Behavioral: Intermittent normoxia

Interventions

The intermittent hypoxia protocol will consist of three 4-minute hypoxic cycles (arterial oxygen saturation of 80%) interspersed with 4-minute normoxic cycles.

Intermittent hypoxia

The intermittent normoxia protocol will consist of three 4-minute normoxic cycles (compressed air) interspersed with 4-minute normoxic cycles (room air).

Intermittent normoxia

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Related Publications (25)

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    PMID: 20351340BACKGROUND
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    PMID: 29785503BACKGROUND
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    PMID: 27707723BACKGROUND
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    PMID: 21239631BACKGROUND
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    PMID: 21840524BACKGROUND
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    PMID: 17724264BACKGROUND
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    PMID: 29672298BACKGROUND
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    PMID: 24189016BACKGROUND
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    PMID: 12796124BACKGROUND
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    PMID: 23604707BACKGROUND
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    PMID: 19013544BACKGROUND
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    PMID: 15262041BACKGROUND
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    PMID: 8335593BACKGROUND
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    PMID: 25389072BACKGROUND
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    PMID: 20689088BACKGROUND

Study Officials

  • Sophie Lalande

    UT Austin

    PRINCIPAL INVESTIGATOR

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

Locations