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A Double-Blind, Randomized, Placebo Controlled, Parallel Group Study to Compare the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen to Placebo in Patients With Stage I and Stage II Hypertension
This 16 week study will examine the ability of olmesartan medoxomil to lower the blood pressure of patients with moderate to severe high blood pressure in comparison to placebo. The medication being tested has been approved by the FDA for the treatment of high blood pressure.
Details
| Lead sponsor | Daiichi Sankyo |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 278 |
| Start date | 2006-12 |
| Completion | 2007-10 |
Conditions
- Hypertension
Interventions
- olmesartan medoxomil + hydrochlorothiazide, if necessary
- Placebo
Primary outcomes
- Change From Baseline in Mean Systolic Blood Pressure (SBP) After 12 Weeks of Randomized Treatment as Measured by Omron Device. — baseline to 12 weeks
The change from baseline in mean systolic blood pressure (SBP) after 12 weeks of randomized treatment was compared between the olmesartan based treatment group and the placebo treatment group.
Countries
United States