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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02913794
Other study ID # BR-FMS-OS-402
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 11, 2016
Est. completion date March 29, 2018

Study information

Verified date June 2023
Source Boryung Pharmaceutical Co., Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fimasartan and Rosuvastatin for hypertension and dyslipidemia control


Recruitment information / eligibility

Status Completed
Enrollment 541
Est. completion date March 29, 2018
Est. primary completion date March 29, 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Hypertension patients who are taking an anti-hypertensive agent, including Fimasartan at least 12 weeks or more. - Dyslipidemia patients who are taking dyslipidemia drug, including Rosuvastatin at least 12 weeks or more - Patients who has blood pressure and lipid levels (Total cholesterol, LDL-C, HDL-C, non-HDL-C, * TG) checks 2 weeks before registration Exclusion Criteria: - Patients being hospitalized - Patients who stop taking Fimasartan or Rosuvastatin within 12 weeks 14 or more consecutive days - Patients who have more than 400mg/dl triglyceride(TG) at the registration time

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Severance Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Boryung Pharmaceutical Co., Ltd

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Co-relation between blood pressure and dyslipidemia Check the blood pressure and dyslipidemia control rates, also check the correlation between these two disease 12 weeks
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