Post Marketing Surveillance Study in Rehabilitation Clinics (Cardio, Nephro, Diabetes, Pulmo)
NCT ID: NCT02262611
Last Updated: 2014-10-13
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
266 participants
OBSERVATIONAL
2003-01-31
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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Hypertension patients - Pneumology
Micardis®
MicardisPlus®
Hypertension patients - Cardiology
Micardis®
MicardisPlus®
Hypertension patients - Nephrology
Micardis®
MicardisPlus®
Hypertension patients - Diabetology
Micardis®
MicardisPlus®
Interventions
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Micardis®
MicardisPlus®
Eligibility Criteria
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Inclusion Criteria
No additional selection criteria have to be considered. Treatment was at the discretion of the physician following the summary of product information for Micardis® and MicardisPlus®
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Boehringer Ingelheim
INDUSTRY
Responsible Party
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Other Identifiers
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502.429, 502.430, 502.431
Identifier Type: OTHER
Identifier Source: secondary_id
502.428
Identifier Type: -
Identifier Source: org_study_id
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