跳至主要内容
临床试验/CTRI/2013/07/003804
CTRI/2013/07/003804已完成未知

ipid target achievement in high risk patients with Coronary Heart Disease (DYSIS II ACS/CHD) - Dysis-II

Merck Co Inc0 个研究点目标入组 10,500 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
Merck Co Inc
入组人数
10,500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • DYSIS II ACS
  • Age >= 18 years
  • Hospitalized for acute coronary syndrome (ACS) (ST segment elevation myocardial infarction (STEMI), left bundle branch block (LBBB), Non-ST elevated myocardial infarction (NSTEMI), unstable angina) at time of enrolment
  • Full lipid profile available based on blood drawn within 24 hours of admission to the hospital.
  • On lipid-modifying therapy (LMT) for equal to or more than 3 months at time of enrolment, or NOT at all on LMT.
  • DYSIS II CHD
  • Age >= 18 years
  • Documented CHD by at least one of the following:
  • o coronary angiography (stenosis >50%)
  • o cardiac computed tomography (CT) (stenosis > 50%)
  • o prior percutaneous coronary intervention (PCI) or prior coronary artery bypass graft (CABG)
  • o history of ACS >3 months prior to enrolment
  • o Complete fasting lipid profile 0-12 months prior to enrollment while on lipid modifying therapy (LMT) for equal to or more than 3 months or not at all on LMT

排除标准

  • DYSIS II ACS
  • Patients treated with lipid-modifying therapy for more than 0 but less than 3 months at the time of enrolment
  • DYSIS II CHD
  • History of ACS within 3 months prior to enrollment
  • Participation in DYSIS II ACS

研究者

发起方
Merck Co Inc

相似试验