N/A
N=22
24-hour Blood Pressure Measurements and Ischemic Conditioning
Blood Pressure
Bottom Line
View on ClinicalTrials.gov: NCT03303404 ↗Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcome: Primary: Change From Baseline in Flow Mediated Dilation After 24 Hour Ischemic Conditioning With Blood Pressure Cuff — 6.6 percentage of baseline
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Ambulatory (24-hour) Blood Pressure (Device)
- Age
- Adult · 30+ yrs
- Sex
- All
- Sponsor
- University of Texas at Austin
- Primary completion
- Sep 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Flow Mediated Dilation After 24 Hour Ischemic Conditioning With Blood Pressure Cuff |
6.6 | — |
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).
Eligibility Criteria
Inclusion Criteria
Adults aged between 30 to 60 years old.
Exclusion Criteria
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.
Data sourced from ClinicalTrials.gov (NCT03303404). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.