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
| Type | Name | Description |
|---|---|---|
| DRUG | Nebivolol | Oral 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.