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
| Type | Name | Description |
|---|---|---|
| DRUG | nebivolol | Encapsulated 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 |
| DRUG | Placebo | Lisinopril 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.