Evaluating the Efficacy and Safety of Co-administrated Rosuvastatin/Ezetimibe and Telmisartan
NCT ID: NCT03872232
Last Updated: 2021-01-15
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
PHASE3
180 participants
INTERVENTIONAL
2019-02-26
2020-08-12
Brief Summary
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Detailed Description
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In "Rosuvastatin/Ezetimibe+Telmisartan" treatment group, 60 subjects will be assigned and the subjects administer "Rosuvastatin/Ezetimibe+Telmisartan" for 8 weeks.
In "Rosuvastatin/Ezetimibe" treatment group, 60 subjects will be assigned and the subjects administer "Rosuvastatin/Ezetimibe" for 8 weeks.
In "Telmisartan" treatment group, 60 subjects will be assigned and the subjects administer "Telmisartan" for 8 weeks.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Ezetimibe/Rosuvastatin and Telmisartan
60 subjects will be assigned and the subjects will be administered "Ezetimibe/Rosuvastatin and Telmisartan" for 8 weeks.
Ezetimibe/Rosuvastatin
PO, Once daily(QD), 8weeks
Telmisartan
PO, Once daily(QD), 8weeks
Ezetimibe/Rosuvastatin
60 subjects will be assigned and the subjects will be administered "Ezetimibe/Rosuvastatin" for 8 weeks.
Ezetimibe/Rosuvastatin
PO, Once daily(QD), 8weeks
Telmisartan
60 subjects will be assigned and the subjects will be administered "Telmisartan" for 8 weeks.
Telmisartan
PO, Once daily(QD), 8weeks
Interventions
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Ezetimibe/Rosuvastatin
PO, Once daily(QD), 8weeks
Telmisartan
PO, Once daily(QD), 8weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Subjects with hypertension and hyperlipidemia
Exclusion Criteria
* Other exclusions applied
19 Years
ALL
No
Sponsors
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Addpharma Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Hyo Soo Kim, M.D., Ph.D
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Hospital
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Other Identifiers
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ROZETEL_RCT
Identifier Type: -
Identifier Source: org_study_id
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