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Obesity is a global health concern that is associated with high blood pressure and an increased risk for developing cardiovascular disease. The purpose of this study is to find out if the investigational drug angiotensin-(1-7) can improve cardiovascular health in people with obesity and high blood pressure.
A randomized, double blind, placebo controlled, crossover study will be conducted to determine if acute intravenous angiotensin-(1-7) infusion reduces cardiovascular sympathetic tone and blood pressure and improves the function of blood vessels in participants with obesity hypertension. This is an outpatient study that requires a screening visit, and if eligible, two study visits separated by at least one week in the Clinical Research Center within the Penn State Milton S. Hershey Medical Center. The study visits will include intravenous infusion of angiotensin-(1-7) or saline for approximately two hours, starting with increasing doses and holding at a steady-state dose. Endothelial function will be measured and blood samples collected at baseline and at the end of infusion. Blood pressure, heart rate, and muscle sympathetic nerve activity (via microneurography) will be measured continuously throughout the study. Each study visit will last approximately 4 hours.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Penn State Milton S. Hershey Medical Center
Hershey, Pennsylvania, United States
Start Date
January 23, 2025
Primary Completion Date
March 1, 2029
Completion Date
March 1, 2029
Last Updated
September 19, 2025
52
ESTIMATED participants
Angiotensin-(1-7)
DRUG
Saline
DRUG
Lead Sponsor
Milton S. Hershey Medical Center
Collaborators
NCT02417740
NCT01143454
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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