Status:

COMPLETED

24-hour Blood Pressure Measurements and Ischemic Conditioning

Lead Sponsor:

University of Texas at Austin

Conditions:

Blood Pressure

Eligibility:

All Genders

30-60 years

Phase:

NA

Brief Summary

To determine if 24-hr ambulatory blood pressure monitoring effects endothelial function, we will measure flow-mediated dilation before and after the blood pressure monitoring (ischemia conditioning).

Detailed Description

Reestablishing blood flow (reperfusion) to organs that had their blood supply restricted (ischemia) can cause damage to the vasculature via injury and tissue death resulting in endothelial dysfunction...

Eligibility Criteria

Inclusion

  • Adults aged between 30 to 60 years old.

Exclusion

  • Exclusion from the study may be due to: i) pregnancy (by asking the subjects when the last time she had menstruation; we do have simple testing kits available if a subject is unsure about her status); ii) a recent illness, recent surgery, or any medical intervention in the 48 hours before any of the study days; iii) personal history of diabetes (fasting blood glucose \> 126 mg/dL), heart disease, or other cardiovascular problems.

Key Trial Info

Start Date :

September 12 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 20 2018

Estimated Enrollment :

22 Patients enrolled

Trial Details

Trial ID

NCT03303404

Start Date

September 12 2017

End Date

September 20 2018

Last Update

December 22 2020

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Dr. Hirofumi Tanaka

Austin, Texas, United States, 78713

24-hour Blood Pressure Measurements and Ischemic Conditioning | DecenTrialz