跳至主要内容
临床试验/NCT02913794
NCT02913794已完成不适用

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

Boryung Pharmaceutical Co., Ltd1 个研究点 分布在 1 个国家目标入组 541 人开始时间: 2016年10月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
541
试验地点
1
主要终点
Co-relation between blood pressure and dyslipidemia

研究概览

简要总结

Fimasartan and Rosuvastatin for hypertension and dyslipidemia control

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Co-relation between blood pressure and dyslipidemia

时间窗: 12 weeks

Check the blood pressure and dyslipidemia control rates, also check the correlation between these two disease

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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