Assessment of Compliance With Antihypertensive Telmisartan Therapy
NCT ID: NCT00470886
Last Updated: 2012-11-16
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
3400 participants
OBSERVATIONAL
2007-04-30
2010-01-31
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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Group 1
Telmisartan (Kinzal/Pritor, BAY68-9291)
Primary care clinic hypertensive patients for whom physician decided to start the treatment with telmisartan
Interventions
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Telmisartan (Kinzal/Pritor, BAY68-9291)
Primary care clinic hypertensive patients for whom physician decided to start the treatment with telmisartan
Eligibility Criteria
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Inclusion Criteria
* Untreated or ineffectively treated arterial hypertension
Exclusion Criteria
* Allergy to Telmisartan
* Pregnancy and lactation period
* Unwillingness to participate in the study
* Inability to use the drug reminder device
* Unwillingness to use the drug reminder device
18 Years
ALL
No
Sponsors
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Bang & Olufsen Medicom
INDUSTRY
Bayer
INDUSTRY
Responsible Party
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Bayer Sp. z o.o.
Principal Investigators
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Bayer Study Director
Role: STUDY_DIRECTOR
Bayer
Locations
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Many Locations, , Poland
Many Locations, , Slovakia
Countries
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Other Identifiers
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KL0710PL
Identifier Type: OTHER
Identifier Source: secondary_id
14237 - KL0710SK
Identifier Type: OTHER
Identifier Source: secondary_id
12827
Identifier Type: -
Identifier Source: org_study_id
NCT00458692
Identifier Type: -
Identifier Source: nct_alias