EUCTR2004-002077-23-AT
Active, not recruiting
Not Applicable
Efficacy and safety of Olmesartan medoxomil in elderly patients with mild to moderate hypertension
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Male or female outpatients, aged 65-89 years, with mild to moderate essential hypertension (sDBP>=90mmHg and sSBP>=140mmHg)
- Sponsor
- MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG S.A.
- Enrollment
- 390
- Status
- Active, not recruiting
- Last Updated
- 13 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients of both sexes responding to the following criteria will be enrolled:
- •–age \>65 and \<89 years;
- •–new diagnosis of Grade 1 or 2 essential arterial hypertension (systolic arterial pressure when seated 140\-179 mmHg and diastolic arterial pressure when seated 90\-109 mmHg);
- •essential arterial hypertension Grade 1 or 2 not controlled with current treatment or with intolerance to current treatment;
- •–absence of contraindications with use of Olmesartan medoxomil and Ramipril;
- •–letter of informative notes for patient and signature of informed consent;
- •–patient residence stable and compatible with the study’s needs;
- •–willingness to respect the medical controls planned in the protocol.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
Exclusion Criteria
- •–Grade 3 essential arterial hypertension (systolic arterial pressure when seated ³ 180 mmHg and/or diastolic arterial pressure when seated ³ 110 mmHg);
- •–secondary or malign arterial hypertension;
- •–unstable angina;
- •–Atrial fibrillation;
- •–Frequent ventricular ectopic beats or other arrhytmias which could interfere with blood pressure recording ;
- •–cardiac arrhythmia requiring administration of anti\-arrhythmic medicines;
- •–heart failure requiring medical treatment;
- •–myocardial infarction in the previous 6 months;
- •–cerebrovascular events in the previous 6 months;
- •–haemodynamically significant valvulopathy;
Outcomes
Primary Outcomes
Not specified
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