KCT0008033招募中未知
Prasugrel Monotherapy versus Combination of Clopidogrel plus Aspirin in Stabilized Patients with Acute Coronary Syndrome after Complex High-risk and Indicated Percutaneous Coronary Intervention (PRADO-CHIP)
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 2,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 74(Year)(—)
- 性别
- All
入选标准
- •1)Patient must be at least 19 years of age
- •2)Patients with ACS: unstable angina, non ST-segment elevation MI (NSTEMI), or ST-segment elevation MI (STEMI)
- •3)Patients undergoing Complex High-risk and Indicated Percutaneous Coronary Intervention(CHIP)
- •*Definition of CHIP
- •1.Significant left main (LM) diseases including ostial, body or distal LM bifurcation diseases
- •2.Ostial stenosis of left anterior descending or left circumflex arteries
- •3.Bifurcation lesions treated with 2 stents
- •4.Chronic total occlusion
- •5.Severe calcified lesion: encircling calcium on coronary angiography
- •6.Multi-vessel disease involving PCI done in at least two vessels
- •7.More than 3 stents implanted
- •8.Diffuse long lesion of more than 38 mm
- •9.CABG patients: native and/or graft vessels
- •4) For female patients of childbearing age, those who consent to pregnancy testing and adherence to highly effective birth control methods from enrollment to 5 days after study completion
- •5) Patients who can verbally confirm understandings of the study objective and clinical follow-up required in this registry, and he/she or his/her legally authorized representative provides written informed consent prior to the study commitment
排除标准
- •1) Patients who do not give their consent to join the study or patients who are deemed unsuitable for the study by the investigator
- •2) Patients with a history of cerebral hemorrhage, transient ischemia attack, or ischemic stroke
- •3) Patients scheduled for staged PCI
- •4) Patients with significant active bleeding, bleeding diathesis, and/or coagulopathies (Hb < 10 g/dL before correction, bleeding requiring transfusion in the prior 30 days, abdominal/thoracic/neural surgery in the prior 90 days, patients at high risk for injuries)
- •5) Patients who are hypersensitive to contrast mediums or antiplatelet drugs (aspirin, clopidogrel, prasugrel)
- •6) Patients with moderate to severe liver dysfunction (Child Pugh class C)
- •7) Patients with a life expectancy < 1 year due to non-cardiac disease
- •8) Patients needing anticoagulation (warfarin, DOAC; direct oral anticoagulant)
- •9) Pregnant and/or breast feeding patients
- •10) Patients with galactose intolerance, lactase deficiency, and/or glucose-galactose malabsorption)
- •11) Patients with major ischemic and/or bleeding events within 1 months after index PCI will be excluded
- •12) Patents aged 75 years or above
研究者
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