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
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
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