Study of the Efficacy and Safety of Nebivolol in Younger Patients (18 - 54 Years)

Completed · Phase 4 · Has a placebo group

Conditions studied: Hypertension

In brief

The purpose of this study is to assess the efficacy, safety, and tolerability of 8 weeks of therapy with nebivolol in comparison to placebo in younger patients 18 - 54 years of age with stage 1 or stage 2 essential hypertension.

Key facts

Study ID
NCT01415531
Run by
Forest Laboratories
People needed
641
Starts
2011-08-01
Expected to finish
2012-04-01
Last updated by the study team
2013-05-16

Who can join

Age: 18 and older, up to 54. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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