Clinical Trials Directory

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

TypeNameDescription
DRUGNebivololEncapsulated Nebivolol 5 mg, 10 mg, 20, mg, 40 mg total daily dosage, oral administration once daily
DRUGCarvedilolEncapsulated 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.