Blood Brain Flow and Exercise
Cerebral Vasodilator Responses in Sedentary and Exercise Trained Humans
5 other identifiers
interventional
80
1 country
1
Brief Summary
Cerebral vasodilator responses to CO2 will be measured in young healthy adults, healthy sedentary older adults, and healthy exercise trained older adults. This variable will be examined before and after administering the cyclooxygenase inhibitor indomethacin, which has been shown to blunt cerebral vasodilator responses. In addition, the investigators will examine these counter-regulatory hemodynamic mechanisms to hypoperfusion caused by indomethacin.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for early_phase_1
Started Jun 2016
Typical duration for early_phase_1
1 active site
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
First Submitted
Initial submission to the registry
December 22, 2015
CompletedFirst Posted
Study publicly available on registry
January 12, 2016
CompletedStudy Start
First participant enrolled
June 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2019
CompletedDecember 18, 2019
December 1, 2019
2.8 years
December 22, 2015
December 13, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Cerebral Vasodilator Responses
Utilize a Transcranial Doppler to measure blood flow velocity in response to inhaled carbon dioxide.
Measurement at baseline
Secondary Outcomes (2)
Cerebral Vasodilator Responses
Measurement beginning 60 minutes post drug and measured through 180 minutes
Blood Pressure
Measurement at baseline and beginning 60 minutes post drug and measured through 180 minutes
Study Arms (1)
Drug
EXPERIMENTALControl-Hypercapnic Trials: Three stepwise CO2 elevations will be applied to the patient by adding fractional concentration of inspired CO2 (FICO2) at 2%, 4%, and 6% each time, balanced with room air. The end tidal CO2 (PetCO2) will be elevated and maintained constant for three minutes at each target level. Breath-by-breath changes in minute ventilation (VE) and PetCO2 will be measured. Drug-Indomethacin: Healthy volunteers, indomethacin suspension will be orally administered at 1.2 mg/kg. After drug administration, the patient will rest quietly for 90 minutes.
Interventions
Eligibility Criteria
You may qualify if:
- Young subjects between 18-35 years old
- Older subjects between 55-75 years old
- Nonsmokers
- Physically active (exercise more than 3 times per week for at least 30 minutes)
- Sedentary (no formal exercise over 1 hour per week).
You may not qualify if:
- Outside of the specified age range
- Present with history or evidence of hepatic, renal, or hematological disease; peripheral vascular disease; stroke/neurovascular disease; diabetes; hypertension
- Take medications that indicate hepatic, renal, hematological disease; cardiovascular disease, including hypertension; stroke/neurovascular disease; and diabetes
- Body mass index \>34 kg/m2
- Take physician-prescribed medications that may interact with indomethacin: 1) cardiovascular drugs (e.g. angiotensin-converting-enzyme inhibitor (ACE inhibitors), angiotensin II receptor blockers (ARB's), Diuretics); 2) drugs that would increase bleeding risk (e.g. warfarin, heparin, clopidogrel, rivaroxaban, other NSAIDs); or 3) drugs associated with increased renal toxicity (e.g. cyclosporin, tacrolimus)
- Vulnerable populations (i.e. pregnant women, prisoners, individuals lacking capacity to consent, etc.)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gymnasium-Natatorium
Madison, Wisconsin, 53716, United States
Related Publications (41)
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MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jill N Barnes, PhD
University of Wisconsin, Madison
Study Design
- Study Type
- interventional
- Phase
- early phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 22, 2015
First Posted
January 12, 2016
Study Start
June 1, 2016
Primary Completion
April 1, 2019
Study Completion
April 1, 2019
Last Updated
December 18, 2019
Record last verified: 2019-12
Data Sharing
- IPD Sharing
- Will not share