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临床试验/KCT0008033
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)

The Catholic University of Korea, Seoul St. Mary's Hospital0 个研究点目标入组 2,000 人开始时间: 待定最近更新:
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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