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

Completed · Phase 4 · Has a placebo group

Conditions studied: Hypertension

In brief

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

Key facts

Study ID

NCT00734630

Run by

Forest Laboratories

People needed

491

Starts

2008-08-01

Expected to finish

2010-05-01

Last updated by the study team

2011-04-26

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female, ambulatory outpatients 18-85 years old at screening
• Have a history of hypertension
• Qualifying laboratory results

You may not qualify if…

• Severe hypertension, including chronic kidney disease
• Documented congestive heart failure
• Have clinically significant respiratory, liver, or heart disease
• History of stroke, heart attack, or heart surgery in the last 6 months
• Have a history of hypersensitivity to nebivolol or other beta blockers.

Where it is running

• Forest Investigative Site 092 — Huntsville, Alabama, United States
• Forest Investigative Site 058 — Mesa, Arizona, United States
• Forest Investigative Site 059 — Tempe, Arizona, United States
• Forest Investigative Site 024 — Anaheim, California, United States
• Forest Investigative Site 012 — Bell Gardens, California, United States
• Forest Investigative Site 026 — Chino, California, United States
• Forest Investigative Site 083 — Costa Mesa, California, United States
• Forest Investigative Site 030 — Los Angeles, California, United States
• Forest Investigative Site 053 — Orange, California, United States
• Forest Investigative Site 077 — Riverside, California, United States
• Forest Investigative Site 034 — Sacramento, California, United States
• Forest Investigative Site 028 — Sacramento, California, United States
• Forest Investigative Site 048 — San Bernardino, California, United States
• Forest Investigative Site 075 — Santa Ana, California, United States
• Forest Investigative Site 087 — Santa Ana, California, United States
• Forest Investigative Site 090 — Temecula, California, United States
• Forest Investigative Site 010 — Tustin, California, United States
• Forest Investigative Site 001 — Westlake Village, California, United States
• Forest Investigative Site 061 — Wheat Ridge, Colorado, United States
• Forest Investigative Site 046 — Brooksville, Florida, United States
• Forest Investigative Site 015 — DeLand, Florida, United States
• Forest Investigative Site 035 — Fort Lauderdale, Florida, United States
• Forest Investigative Site 009 — Hialeah, Florida, United States
• Forest Investigative Site 039 — Hollywood, Florida, United States
• Forest Investigative Site 070 — Gulf Shores, Alabama, United States

Full record on ClinicalTrials.gov

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