N/A Completed N=22 Other

24-hour Blood Pressure Measurements and Ischemic Conditioning

Blood Pressure

Source: ClinicalTrials.gov NCT03303404 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Dec 2020

Primary outcomePrimary: Change From Baseline in Flow Mediated Dilation After 24 Hour Ischemic Conditioning With Blood Pressure Cuff — 6.6 percentage of baseline

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).

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	—

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.

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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. Informational only — not medical advice.