Phase 3
N=185
Blood Pressure Lowering Ability and Safety of an Olmesartan and Amlodipine Based Treatment Regimen in Patients With Stage I and Stage II Hypertension
Hypertension
Bottom Line
View on ClinicalTrials.gov: NCT00527514 ↗Enrolled (actual)
185
Serious AEs
0.3%
Results posted
Sep 2009
Primary outcome: Primary: Change From Baseline in Mean 24-hour Systolic Blood Pressure Measured by Ambulatory Monitoring — -21.4 mm Hg — p=<0.0001
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Amlodipine (Drug); Olmesartan medoxomil plus amlodipine (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Daiichi Sankyo
- Primary completion
- Apr 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Mean 24-hour Systolic Blood Pressure Measured by Ambulatory Monitoring |
-21.4 | <0.0001 sig |
| SECONDARY Change From Baseline in Daytime and Nighttime Ambulatory Systolic Blood Pressure |
-23.1; -18.5 | <0.0001 sig |
| SECONDARY Change From Baseline in Cuff Systolic Blood Pressure for the Amlodipine 5mg Group. |
-10.1 | <0.0001 sig |
| SECONDARY Change From Baseline in Cuff Systolic Blood Pressure for the Amlodipine 5mg + Olmesartan 20 mg Group. |
-18.0 | <0.0001 sig |
| SECONDARY Change From Baseline in Cuff Systolic Blood Pressure for the Amlodipine 5mg + Olmesartan 40 mg Group |
-20.5 | <0.0001 sig |
| SECONDARY Change From Baseline in Cuff Systolic Blood Pressure for the Amlodipine 10 mg + Olmesartan 40 mg Group |
-24.6 | <0.0001 sig |
Summary
This study will be conducted to assess the efficacy and safety of an amlodipine/olmesartan treatment regimen in stage 1 and stage 2 hypertensive subjects.
Eligibility Criteria
Inclusion Criteria
- Males or females greater than or equal to 18 years of age
- Patients with a mean seated systolic blood pressure (MSSBP) greater than or equal to 140 mm Hg but less than or equal to 199 mm Hg or a mean seated diastolic blood pressure (MSDBP) greater than or equal to 90 mm Hg and less than or equal to 109 mm Hg, following a period of taking only placebo
- Patients with a mean daytime (8AM-4PM) systolic blood pressure greater than or equal to 135 mm Hg and less than or equal to 199 mm Hg and a mean daytime diastolic blood pressure less than or equal to 109 mm Hg as measured by an ambulatory blood pressure monitoring device (ABPM), after a period of taking only placebo
- If female, must have negative serum pregnancy test at screening and be either post-menopausal (greater than or equal to 1 year), had a hysterectomy or tubal ligation at least 6 months before consent or if of childbearing potential, must practice approved measures of birth control throughout study
Exclusion Criteria
- History of stroke or transient ischemic attack (TIA) within the last one year
- History of myocardial infarction, coronary angioplasty, coronary artery bypass graft, or heart failure within the past 6 months
- Patients with secondary hypertension of any etiology, such as renal disease, pheochromocytoma, or Cushing's syndrome
- Type I diabetes. Patients with Type II diabetes on stable treatment, with fasting glucose <160 mg/dl may enroll
- Patients with hemodynamically significant cardiac valvular disease
- Patients with clinically significant cardiac conduction defects, including second or third degree AV block, left bundle branch block, sick sinus syndrome, atrial fibrillation, atrial flutter, an accessory bypass tract, or any arrhythmia requiring medication
Data sourced from ClinicalTrials.gov (NCT00527514). 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.