Impact of MK-0954A on Uric Acid in the Management of Hypertension (MK-0954A-366)
NCT ID: NCT01368185
Last Updated: 2022-02-09
Study Results
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View full resultsBasic Information
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COMPLETED
1705 participants
OBSERVATIONAL
2008-11-30
2010-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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All Participants
Participants with hypertension who had been treated with MK-0954A (losartan potassium 50 mg + hydrochlorothiazide 12.5 mg) for at least three months
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Diagnosed with hypertension and had received MK-0954A 50/12.5 mg for at least 3 months
* Had at least one serum uric acid measurements at baseline and one at 3 months after using MK-0954A 50/12.5 mg
* Had the following records documented in the chart during the data collection period:
* medical history and co-morbidities (if available)
* sitting blood pressure, serum uric acid, lipid profile test results before and after using MK-0954A 50/12.5 mg
* serum electrolytes, serum creatinine, and pre-meal sugar (if available)
* prescription information of all antihypertensive regimens
Exclusion Criteria
* Serum creatinine \>2 mg/dL
20 Years
75 Years
ALL
No
Sponsors
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Organon and Co
INDUSTRY
Responsible Party
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Other Identifiers
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MK-0954A-366
Identifier Type: -
Identifier Source: secondary_id
0954A-366
Identifier Type: -
Identifier Source: org_study_id
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