NCT02248129
Completed
Not Applicable
Pharmaco-epidemiological Study Describing a Population of Hypertensive Patients Treated in General Practice With a Fixed-dose Combination of Telmisartan and Hydrochlorothiazide, the Level of Blood Pressure Control and the Modalities of Arterial Hypertension Management
ConditionsHypertension
InterventionsTelmisartan and hydrochlorothiazide
Overview
- Phase
- Not Applicable
- Intervention
- Telmisartan and hydrochlorothiazide
- Conditions
- Hypertension
- Sponsor
- Boehringer Ingelheim
- Enrollment
- 4255
- Primary Endpoint
- Percentage of patients with low blood pressure
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
Study to compare the level of blood pressure control in hypertensive, hypertensive diabetics and hypertensive with renal insufficiency (observed data) in the study population, with the objectives of the High Authority for Health recommendations (benchmark)
Investigators
Eligibility Criteria
Inclusion Criteria
- •Hypertensive patients already treated for at least 1 month with Telmisartan plus hydrochlorothiazide, consulting the physician consecutively for whatever reason
Exclusion Criteria
- Not provided
Arms & Interventions
Hypertensive patients
Intervention: Telmisartan and hydrochlorothiazide
Outcomes
Primary Outcomes
Percentage of patients with low blood pressure
Time Frame: up to 4 weeks
lower than 140/90 mmHg in the general population of hypertensive patients, hypertensive diabetics and hypertensive with renal insufficiency
Secondary Outcomes
- Number of patients with adverse events(up to 4 weeks)
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