Status:
COMPLETED
The Effect of Nebivolol in Hypertensive Patients With Coronary Artery Disease
Lead Sponsor:
Forest Laboratories
Conditions:
Hypertension
Coronary Artery Disease
Eligibility:
All Genders
18-80 years
Phase:
PHASE4
Brief 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 patie...
Eligibility Criteria
Inclusion
- Male or female ambulatory outpatients 18 to 85 of age at screening
- Coronary artery disease as defined by: status post myocardial infarction (heart attack) greater than 14 days post event with no upper time limit (and followed by stress testing with additional imaging (echocardiographic or nuclear) within the 12 months prior to enrollment) and/or angiographic evidence of one or more major coronary arteries narrowing of greater than 50% and/or a history of percutaneous or surgical coronary revascularization greater than 4 months after that procedure at the time of enrollment.
- Qualifying blood pressure criteria for study entry and for randomization
- Willing to adhere to exercise stress (treadmill) tests
Exclusion
- Unstable angina within 7 days of screening
- Potential coronary surgical/intervention within the next 6 months
- Have any form of secondary hypertension
- Have a history of hypersensitivity to nebivolol, metoprolol, carvedilol, or any beta blocker
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
39 Patients enrolled
Trial Details
Trial ID
NCT00673075
Start Date
May 1 2008
Last Update
September 28 2010
Active Locations (34)
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1
Forest Investigative Site
Birmingham, Alabama, United States, 35294
2
Forest Investigative Site
Peoria, Arizona, United States, 85381
3
Forest Investigative Site
Buena Park, California, United States, 90620
4
Forest Investigative Site
Los Angeles, California, United States, 90048