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临床试验/NCT00723723
NCT00723723已完成不适用

Compliance With LDL-Lowering Therapy For Secondary Prevention of Coronary Heart Disease in Real Life Practice

Organon and Co0 个研究点目标入组 555 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
555
主要终点
percentage of patients reaching target LDL levels

研究概览

简要总结

This observational study is being conducted in patients receiving statin treatment as secondary prevention of coronary heart disease under the current standard of care in compliance with European guidelines. The purpose of the study is to evaluate the percentage of these patients that reach target LDL levels. Additionally this study will measure the patient's compliance to treatment as assessed by counting the returned tablets. Both assessments will be made at visits conducted 6-8 weeks after the first visit and 28-32 weeks after the first visit.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • willingness to participate in the study
  • 18 years of age or more
  • clinically established cardiovascular disease to be considered as patients in secondary prevention
  • prior therapy with any statin without achieving goal (2.5 mmol/L of LDL cholesterol) at last lipid check performed

排除标准

  • 未提供

研究组 & 干预措施

Patients with coronary heart disease

Patients being treated with a statin for secondary prevention of coronary heart disease

干预措施: Statin (Drug)

结局指标

主要结局

percentage of patients reaching target LDL levels

时间窗: 6-8 weeks after first visit and 28-32 weeks after first visit

次要结局

  • measure patient compliance to treatment as assessed by counting returned tablets(6-8 weeks after first visit and 28-32 weeks after first visit)

研究者

申办方类型
Industry
责任方
Sponsor

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