跳至主要内容
临床试验/EUCTR2009-014176-22-PL
EUCTR2009-014176-22-PL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 - ACCOAST

Eli Lilly and Company0 个研究点目标入组 4,100 人开始时间: 2009年11月13日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
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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