NCT02653638

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

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P75+ for early_phase_1

Timeline
Completed

Started Jun 2016

Typical duration for early_phase_1

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

First Submitted

Initial submission to the registry

December 22, 2015

Completed
21 days until next milestone

First Posted

Study publicly available on registry

January 12, 2016

Completed
5 months until next milestone

Study Start

First participant enrolled

June 1, 2016

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2019

Completed
Last Updated

December 18, 2019

Status Verified

December 1, 2019

Enrollment Period

2.8 years

First QC Date

December 22, 2015

Last Update Submit

December 13, 2019

Conditions

Keywords

Cerebral Vasodilator FunctionWhite Matter Hyperintensity VolumeDefault Mode Network ConnectivityCognitive FunctionCardiorespiratory FitnessAging

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

EXPERIMENTAL

Control-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.

Other: ControlDrug: Indomethacin

Interventions

ControlOTHER

1. Transcranial Doppler 2. Blood Pressure 3. Heart Rate 4. Oxygen Saturation

Drug

1. Transcranial Doppler 2. Blood Pressure 3. Heart Rate 4. Oxygen Saturation

Drug

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Related Publications (41)

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MeSH Terms

Interventions

Indomethacin

Intervention Hierarchy (Ancestors)

IndolesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Jill N Barnes, PhD

    University of Wisconsin, Madison

    PRINCIPAL INVESTIGATOR

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

Locations