Fimasartan and Rosuvastatin for hypertension and dyslipidemia control
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Full eligibility criteria for NCT02913794
Ages eligible for Study
19 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
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
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
All locations for NCT02913794
Korea, Republic of (1)
Seoul, Korea, Republic of
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Tris trial is registered with FDA with number: NCT02913794. The sponsor of the trial is Boryung Pharmaceutical Co., Ltd and it is looking for 1056 volunteers for the current phase.
Official trial title: A Single-center Cross-sectional Study to Evaluate the Effectiveness of Antihypertensive Treatment Including Fimasartan and the Dyslipidemia Treatment Including Rosuvastatin and to Assess the Association Between the Two Treatments
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