Survey to Assess Why People Are Not Responding to Treatment in Hypertension
NCT ID: NCT01071681
Last Updated: 2011-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1589 participants
OBSERVATIONAL
2009-11-30
2010-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Group 1
Telmisartan (Kinzal/Pritor, BAY68-9291)
Patients under daily life treatment receiving Pritor according to local drug information.
Interventions
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Telmisartan (Kinzal/Pritor, BAY68-9291)
Patients under daily life treatment receiving Pritor according to local drug information.
Eligibility Criteria
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Inclusion Criteria
* Hypertensive patients
* Uncontrolled hypertension (blood pressure \>/=140/90 mmHg on the day of consultation or \>/=130/80 mmHg in diabetic patients or in patients suffering from kidney failure, or in elderly patients with a systolic blood pressure \>/=150 mmHg (in the absence of orthostatic hypotension)
* Patients treated with a combination, fixed or not, of Renin-Angiotensin System Blocker (RASB) + Hydrochlorothiazide (HCTZ)
* Patients examined in common medical care practice, whatever the reason for consultation
* Patients informed of the study
18 Years
ALL
No
Sponsors
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International Clinical Trials Association
OTHER
Bayer
INDUSTRY
Responsible Party
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Bayer Schering Pharma AG
Principal Investigators
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Bayer Study Director
Role: STUDY_DIRECTOR
Bayer
Locations
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Many Locations, , France
Countries
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Other Identifiers
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KL0911FR
Identifier Type: OTHER
Identifier Source: secondary_id
BI INTENS
Identifier Type: OTHER
Identifier Source: secondary_id
14675
Identifier Type: -
Identifier Source: org_study_id