Clinical Trials Directory

Trials / Completed

CompletedNCT01202175

Effects of the Beta-blocker Nebivolol (Bystolic) on Subjects With High Normal Blood Pressure and/or a Family History of Hypertension

Effects of the Novel Beta-adrenergic Antagonist Nebivolol (Bystolic) on Prehypertensive Subjects at Genetic Risk of Hypertension: Implications for Inflammation, Endothelial Dysfunction, and Oxidative Stress.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
University of California, San Diego · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The investigators aim to evaluate subjects at high risk of future development of hypertension, those with a family history of hypertension and/or that already have high normal(SBP 120-139 mmHg or DBP 80-89 mmHg) blood pressure. The investigators plan to investigate whether these subjects have the same markers (such as microscopic protein in the urine or C-reactive protein in the blood) in the blood and urine that people with high blood pressure have, and whether they are improved before and after taking the beta-blocker nebivolol.

Conditions

Interventions

TypeNameDescription
DRUGNebivololOral nebivolol 2.5-5mg once daily

Timeline

Start date
2010-07-01
Primary completion
2012-06-01
Completion
2013-06-01
First posted
2010-09-15
Last updated
2019-08-21
Results posted
2019-08-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01202175. Inclusion in this directory is not an endorsement.