A Study of the Safety and Efficacy of Nebivolol in Hypertensive Patients
Completed · Phase 3
Conditions studied: Hypertension
In brief
A study to determine the safety, efficacy and superiority of nebivolol to placebo for the treatment of elevated blood pressure in patients with mild to moderate hypertension.
Key facts
- Study ID
- NCT00200473
- Run by
- Mylan Bertek Pharmaceuticals
- People needed
- 800
- Starts
- 2001-09-01
- Expected to finish
- 2003-03-01
- Last updated by the study team
- 2005-09-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- An average sitting diastolic blood pressure of greater then or equal to 95 mmHg and less then or equal to 109 mmHg at baseline
You may not qualify if…
- Recent myocardial infarction or stroke
- Secondary hypertension
- Contraindications to beta-blocker therapy or discontinuation of prior antihypertensive agents
- Pregnancy, nursing or women of childbearing age not using appropriate contraception
Where it is running
- Mylan Pharmaceuticals Inc. — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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