drugset / Trial / NCT01057251
Nebivolol in Patients With Systolic Stage 2 Hypertension
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nebivolol | Other / unclassified | 5 mg | Oral |
| Subject | Nebivolol | Other / unclassified | 20 mg | Oral |