跳至主要内容
临床试验/EUCTR2010-021591-28-IT
EUCTR2010-021591-28-IT进行中(未招募)不适用

A clinical trial comparing cangrelor to clopidogrel standard of care therapy in subjects who require percutaneous coronary intervention - Phoenix

THE MEDICINES COMPANY0 个研究点目标入组 10,900 人开始时间: 2011年2月3日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
10,900

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

  • Patients with at least 18 years of age with stable angina (SA), acute coronary syndrome without ST-segment elevation (NSTE-ACS) and myocardial infarction with ST-segment elevation (STEMI) requiring ICP and who have not previously taken an inhibitor of P2Y12.
  • 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

  • 1.Receipt of any P2Y12 inhibitor at any time in the 7 days preceding randomization; 2.Eptifibatide and tirofiban usage within 12 hours preceding randomization (most recent dose must have been administered =12 hours prior to randomization); 3.Abciximab usage within 7 days preceding randomization; 4.Receipt of fibrinolytic therapy in the 12 hours preceding randomization

研究者

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