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临床试验/JPRN-UMIN000019424
JPRN-UMIN000019424已完成4 期

Safety and eficity of 2.5mg prasugrel therapy in the eldely or low body weight Japanese patients undergoing percutaneous coronary intervention - 2.5mg Prasugrel therapy in the eldely or low body weight Japanese patients

Chiba University Hospital0 个研究点目标入组 70 人开始时间: 2015年10月21日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients with contraindications to prasugrel 2. Patients who have severe liver problem 3. Patients who have severe kidney problem 4. History of stroke or transient ischemic attack 5. low platelet counts (less than 10*10^4) 6. Patients who are taking anticoagulants 7. Patients who are planned to administer thrombolytic agents 8. Patients scheduled for PCI or CABG during this study 9. Patients who are taking ticlopidine or cilostazol or prasugrel. 10. Patients judged as inappropriate for trial entry

研究者

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Safety and eficity of 2.5mg prasugrel therapy in the... | 临床试验