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临床试验/NCT01897883
NCT01897883已完成不适用

Dyslipidemia Management in Chinese Post Stroke Patients

AstraZeneca1 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2013年7月最近更新:
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
5,000
试验地点
1
主要终点
To observe LDL-C level of China post-stroke patients within 6-12 months from attack

研究概览

简要总结

The purpose of this study is to provide current and reliable data of dyslipidimia management together with control situation of blood pressure and glucose for post-stroke patients within 6-12 months from attack, and also the association between patient characteristics and control rate of lipids in this population.

It is an non-interventional study, no study specified treatment is required.Approximately 5000 post ischemic stroke patients within 6-12 months from attack will enter into the study. Fifty centres from different regions of China will participate in this study.

详细描述

This is a multicentre, cross-sectional, observational study, aiming to investigate the prevalence and control situation of dyslipidimia in China post ischemic stroke patients within 6-12 months from attack. Patients will be screened consecutively, eligible subjects will be interviewed by investigator and finish a questionire during the visit. Investigator will collect relevant medical history, physical exam results and lab test results including blood lipid (i.e. Triglyceride, Total Cholesterol, LDL-C, HDL-C) and glucose(HbA1c if available).Approximately 5000 post ischemic stroke patients within 6-12 months from attack will enter into the study. Fifty centres from different regions of China will participate in this study.

研究设计

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

入排标准

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

入选标准

  • Male or female with age ≥ 18 years
  • Post ischemic stroke patients within 6-12 months from attack
  • written informed consent is provided to participant in the study

排除标准

  • Significant medical or psychological condition that make patients can not finish the questionnaire independently or with the aids of his/her legal representatives
  • The patient is or will be in another clinical study
  • Previous enrolment in the present study

结局指标

主要结局

To observe LDL-C level of China post-stroke patients within 6-12 months from attack

时间窗: Up to 12 months

Investigator will collect lab test results including blood lipid (i.e. Triglyceride, Total Cholesterol, LDL-C, HDL-C) during the patient visit.

To observe control rate of LDL-C of China post-stroke patients within 6-12 months from attack

时间窗: Up to 12 months

次要结局

未报告次要终点

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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