EUCTR2008-004131-38-FR进行中(未招募)不适用
The ITALIC StudyIs There A LIfe for DES after discontinuation of Clopidogrel : The ITALIC Study - ITALIC
French Society of Cardiology0 个研究点开始时间: 2008年8月4日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •- Male or female subject =18 years of age eligible for PCI with at least one DES Xience implanted in all clinical situations excluding primary PCI for acute MI and treatment of the left main artery.
- •- Male or female subject =18 years of age eligible for PCI with at least one DES Xience.
- •- Patient not pre-treated with abxicimab or eptifibatide during hospitalization
- •- Patient pre-treated with aspirin and clopidogrel before PCI
- •- ASA check at least 24 hours after the interruption of tirofiban
- •- The subject has given written informed and dated consent to participate in this study.
- •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
- •- Subjects not able to give informed consent
- •- Known platelets< 100 000/µl or known hemorrhagic diathesis
- •- Oral anticoagulation or treatment with abxicimab or eptifibatide during hospitalization
- •- ASA check less than 24 hours after the interruption of tirofiban
- •- Thrombolytic therapy within 4 days before ASA check
- •- Contra-indication to aspirin or clopidogrel
- •- Recent major surgery <6 weeks
- •- Evidence of an active gastrointestinal or urogenital bleeding
- •- Severe liver insufficiency
- •- Primary PCI for acute MI
- •- Left main PCI
- •- Any scheduled surgery during the year after enrolment
- •- Severe concomitant disease with life expectation < two years
研究者
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