EUCTR2009-014176-22-FI进行中（未招募）不适用
A Comparison of Prasugrel at the Time of Percutaneous Coronary Intervention (PCI) Or as Pre-treatment At the Time of Diagnosis in Patients with Non-ST-Elevation Myocardial Infarction (NSTEMI) - The ACCOAST Study - TADF
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- Eli Lilly
- 入组人数
- 4,100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •NSTEMI with elevated troponin
- •Scheduled for early coronary angiography and PCI
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Cardiogenic shock at time of randomisation
- •refractory ventricular arrhythmias
- •congestive heart failure
- •cardiac arrest
- •prior TIA or stroke
- •active pathological bleeding
- •severe hepatic impairment
研究者
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