Phase 3
Completed N=130
Olmesartan Medoxomil Versus Losartan in Patients With Hypertension
Source: ClinicalTrials.gov NCT00857285 ↗Enrolled (actual)
130
Serious AEs
—
Results posted
Jul 2009
Primary outcomePrimary: Mean Change of Sitting dBP From Baseline to Week 12 — -14.80; -11.60 mmHg
Summary
The purpose of this study is to determine the efficacy and safety of oral administration of olmesartan medoxomil compared to losartan in subjects with mild to moderate hypertension.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Change of Sitting dBP From Baseline to Week 12 |
-14.80; -11.60 | — |
Eligibility Criteria
Inclusion Criteria
- Diastolic BP 95 mm Hg - 114 mm Hg inclusive
- No participation in any clinical trial for the last 3 months
Exclusion Criteria
- Secondary hypertension
- Malignant hypertension
- Severe arterial hypertension
- Significant cardiovascular disease
- History or clinical evidence of cerebrovascular, gastrointestinal, hematological, hepatic disease, myocardial infarction, or severe liver disorder
- Clinical evidence of renal disease, poorly controlled diabetes, known malabsorption syndromes, psychiatric/emotional problems
Data sourced from ClinicalTrials.gov (NCT00857285). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.