drugset / Trial / NCT00648895

A Study of the Effect of Nebivolol to Evaluate Its Vasodilatory Effects in Hypertensive Patients

NCT00648895

Phase 3 Completed 12 enrolled Forest Laboratories
RandomizedParallel-groupDouble-blindTreatment

Summary

The study is designed to compare the effects of nebivolol (10, 20, 40mg/day) with another beta blocker, extended-release metoprolol, at a range of doses. Its purpose is to study the mechanism of action of nebivolol on forearm blood flow, nitric oxide availability and other biomarkers.

Timeline

Start
2007-11
Primary completion
2009-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Metoprolol ER (TM) Unknown 100 mg Oral
Comparator Metoprolol ER (TM) Unknown 200 mg Oral
Comparator Metoprolol ER (TM) Unknown 400 mg Oral
Comparator Nebivolol Other / unclassified 10 mg Oral
Comparator Nebivolol Other / unclassified 20 mg Oral
Comparator Nebivolol Other / unclassified 40 mg Oral

Indications