Trials / Completed
CompletedNCT00673075
The Effect of Nebivolol in Hypertensive Patients With Coronary Artery Disease
Efficacy and Tolerability of Nebivolol Compared With Carvedilol in Patients With Coronary Artery Disease and Stage I or II Hypertension
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 39 (actual)
- Sponsor
- Forest Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study is being done to see if the blood pressure lowering effect of an approved drug nebivolol is comparable to that of another approved drug carvedilol for the treatment of hypertension in patients who have coronary artery disease.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nebivolol | Encapsulated Nebivolol 5 mg, 10 mg, 20, mg, 40 mg total daily dosage, oral administration once daily |
| DRUG | Carvedilol | Encapsulated Carvedilol 12.5 mg, 25 mg, 50 mg total daily dosage, oral administration twice daily |
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2009-09-01
- First posted
- 2008-05-07
- Last updated
- 2010-09-28
- Results posted
- 2010-09-28
Locations
34 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00673075. Inclusion in this directory is not an endorsement.