Investigation Into the CorrelAtion of pLasma Hs-CRP Concentrations and cardiovascuLar rISk in Korean populaTiOn

AstraZeneca1 个研究点分布在 1 个国家目标入组 1,700 人开始时间: 2009年3月最近更新: 2010年12月6日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方: AstraZeneca
入组人数: 1,700
试验地点: 1
主要终点: Evaluate hs-CRP levels according to risk categories by the NCEP ATP III.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

An observational, non-interventional, multi-centre study to provide further information on the utility of test for a predictive marker by investigating the current prevalence of high sensitivity CRP (hs-CRP) testing and characteristics of each CVD risk group.

研究设计

研究类型: Observational
观察模型: Cohort
时间视角: Retrospective

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Subjects with at least one clinic visit record within the last 12 months from the date of data entry.
•Subjects with at least one hs-CRP level measured within the last 12 months from the date of data entry.

排除标准

•Use of statins or other lipid-lowering therapies including fibrates, niacin, and bile acid sequestrants in the past 3 months prior to hsCRP measurement
•Active inflammatory diseases documented during the period of CRP measurement
•Subjects taking immunosuppressants
•Findings of chronic inflammation: arthritis, lupus, or inflammatory bowel disease

结局指标

主要结局

Evaluate hs-CRP levels according to risk categories by the NCEP ATP III.

时间窗: Within the last 12 months from the date of data entry.

次要结局

Evaluate a relationship between hs-CRP and each CHD CVD risk factor including LDL-C.(Within the last 12 months from the date of data entry.)

研究者

发起方

AstraZeneca

申办方类型

Industry

研究点 (1)

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