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临床试验/JPRN-UMIN000027089
JPRN-UMIN000027089已完成未知

Comparative study to examine the effects of changing between thienopyridine drugs on platelet aggregation activity for patients who are consistently treated with dual antiplatelet therapy: DAPT (clopidogrel + aspirin) over 52 weeks - Comparison of novel antiplatelet agent prasugrel versus clopidogrel in Japanese patients who are consistently treated with DAPT (CONVERT 2)

Kurume University Hospital0 个研究点目标入组 150 人开始时间: 2017年5月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
150

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with bleeding tendency or diathesis thereof 2)Patients with severe hepatic impairment 3)Patients with severe renal impairment 4)Patients with poorly controlled blood pressure receiving antihypertensive therapy. 5)Patients with a history of cerebral infarction or transient ischemic attack 6)Patients with a history of hypersensitivity to thienopyridine drugs such as ticlopidine, prasugrel, clopidogrel. 7)Female who are pregnant, suspected to pregnant, wish to be pregnant, or lactating. 8)Patients who are mentally incompetent (including moderate or serious dementia) and not to gain understanding and cooperation judged by Investigator 9)Patients who are hospitalized during the observation period, or needs to be hospitalized during the research period judged by Investigator. 10)Patients who need to receive treatment with prohibited concomitant drugs during the study 11)Patients disqualified from participation in the study by the principal investigator or study investigators

研究者

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