Expired Study
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Morgantown, West Virginia 26505


Purpose:

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.


Study summary:

This study was a multi-center, multi-national, randomized, double-blind, parallel group, placebo-controlled study of nebivolol over a range of doses in patients with mild to moderate hypertension. The study consisted of 2 phases: screening/washout/single-blind placebo run-in and 2) randomization/double-blind treatment. Patients had 7 scheduled clinic visits during the study.


Criteria:

Inclusion Criteria: - An average sitting diastolic blood pressure of greater then or equal to 95 mmHg and less then or equal to 109 mmHg at baseline Exclusion Criteria: - 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


NCT ID:

NCT00200473


Primary Contact:

Study Director
Betty S. Riggs, MD, MBA
Mylan Pharmaceuticals


Backup Contact:

N/A


Location Contact:

Morgantown, West Virginia 26505
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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