drugset / Trial / NCT01057251

Nebivolol in Patients With Systolic Stage 2 Hypertension

NCT01057251

Phase 4 Completed 433 enrolled Forest Laboratories
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary object of this study is to evaluate the efficacy and safety of 6 weeks of nebivolol monotherapy compared with placebo in patients with systolic stage 2 hypertension.

Timeline

Start
2010-03
Primary completion
2010-12
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Nebivolol Other / unclassified 5 mg Oral
Subject Nebivolol Other / unclassified 20 mg Oral

Indications