Skip to main content
Clinical Trials/EUCTR2004-002077-23-AT
EUCTR2004-002077-23-AT
Active, not recruiting
Not Applicable

Efficacy and safety of Olmesartan medoxomil in elderly patients with mild to moderate hypertension

MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG S.A.0 sites390 target enrollmentMarch 22, 2005

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.

Registry
who.int
Start Date
March 22, 2005
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

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

Similar Trials