跳至主要内容
临床试验/NCT00701402
NCT00701402已完成不适用

Survey on Time to Lipid-lowering Drug Implementation on Dyslipidemic Patients in General Practice.

AstraZeneca1 个研究点 分布在 1 个国家目标入组 3,655 人开始时间: 2008年6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
3,655
试验地点
1
主要终点
time to lipid-lowering drug implementation (immediately, treatment within a period 0-3 month and > 3 month, according to the cardiovascular risk level, (0 risk factor, 1 risk factor, 2 risk factors, ≥ 3 risk factors, secondary prevention).

研究概览

简要总结

The purpose of this observational study is to describe the time to lipid-lowering drug implementation in the management of dyslipidemic patients, according to the cardiovascular risk level.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Diagnosis of dyslipemia made less than 2 years
  • Treated by a lipid-lowering drug
  • Agree to take part in the survey

排除标准

  • Patient included in a clinical trial

结局指标

主要结局

time to lipid-lowering drug implementation (immediately, treatment within a period 0-3 month and > 3 month, according to the cardiovascular risk level, (0 risk factor, 1 risk factor, 2 risk factors, ≥ 3 risk factors, secondary prevention).

时间窗: Once

次要结局

未报告次要终点

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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