Clinical Trials Directory

Trials / Completed

CompletedNCT00734630

Efficacy and Safety of Nebivolol (Added to Lisinopril or Losartan) in Hypertensive Patients

A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Nebivolol Added To Antihypertensive Treatment With Lisinopril or Losartan in Patients With Hypertension.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
491 (actual)
Sponsor
Forest Laboratories · Industry
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This study will assess blood pressure reduction with nebivolol or placebo in patients taking lisinopril or losartan.

Conditions

Interventions

TypeNameDescription
DRUGnebivololEncapsulated Nebivolol 5mg, 10mg, 20mg, or 40mg total daily dosage, oral administration once daily Lisinopril 10mg, 20mg total daily dosage, oral administration Losartan 50mg, 100mg total daily dosage, oral administration
DRUGPlaceboLisinopril 10mg, 20mg total daily dosage, oral administration Losartan 50mg, 100mg total daily dosage, oral administration

Timeline

Start date
2008-08-01
Primary completion
2010-03-01
Completion
2010-05-01
First posted
2008-08-14
Last updated
2011-04-26
Results posted
2011-04-26

Locations

75 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00734630. Inclusion in this directory is not an endorsement.