Post-Marketing Surveillance Of Olmesartan Medoxomil In Combination With Hydrochlorothiazide
NCT ID: NCT00796159
Last Updated: 2009-12-23
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
1723 participants
OBSERVATIONAL
2007-07-31
2008-12-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Olmesartan medoxomil + HCTZ
Olmesartan medoxomil
olmesartan medoxomil 20 mg and HCTZ 12.5 mg
Interventions
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Olmesartan medoxomil
olmesartan medoxomil 20 mg and HCTZ 12.5 mg
Eligibility Criteria
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Inclusion Criteria
* Patient previously taking low-dose medoxomil or any other ARB alone with uncontrolled BP
* Patient with uncontrolled mild to moderate hypertension (SBP\>= 140 and \<=179 mmHg OR DBP of \>=90 and \<=109 mmHg)
Exclusion Criteria
* History of secondary hypertension
18 Years
65 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Pfizer, Inc.
Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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A0021004
Identifier Type: -
Identifier Source: org_study_id