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临床试验/NCT02894255
NCT02894255Unknown4 期

Prospective Multicenter Registry of Hybrid Coronary Artery Revascularization Combined With Surgical Bypass and Percutaneous Coronary Intervention Using Everolimus Eluting Metallic Stents

Teikyo University0 个研究点目标入组 100 人开始时间: 2016年9月最近更新:
适应症

试验速览

阶段
4 期
入组人数
100
主要终点
Major adverse cardiovascular event (death, myocardial infarction, cerebrovascular disorder, and repeat revascularization)

研究概览

简要总结

This prospective multicenter registry evaluates the efficacy of hybrid coronary revascularization (HCR) combining coronary artery bypass surgery (CABG) and percutaneous coronary intervention (PCI) in the treatment of multivessel coronary artery disease. CABG is to be performed in the left anterior descending artery and the left circumflex artery using only arterial grafts, whereas PCI is to be conducted for the treatment of significant stenotic disease in the right coronary artery with everolimus-eluting stents (EESs). This research plans to involve patients scheduled for coronary revascularization for multivessel coronary artery disease who consent to participate in the registry.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with stable angina, unstable angina, or non-ST elevation myocardial infarction.
  • Patients with multivessel coronary artery disease including significant stenotic lesion* in the right coronary artery and also including left main stem disease.
  • Patients who will be referred for CABG.
  • Patients with significant stenotic lesion in the right coronary artery amenable to PCI.
  • Patients who can take DAPT medications.
  • Patients who provided written informed consent. * Significant stenotic lesion means a condition where fractional flow reserve (FFR) is lower than 0.80 or visually confirmed stenosis is at least 75%.

排除标准

  • • Patients with ST elevation myocardial infarction occurring within 24 hours before enrollment.
  • Patients who previously underwent CABG.
  • Patients who are at high risk of receiving CABG.
  • Patients who need simultaneous surgery such as valve surgery other than CABG.
  • Patients with a life expectancy of 1 year or shorter due to co-morbidities.
  • Patients with a history of cerebral infarction within the last 6 months.
  • Patients with congestive cardiac failure of NYHA 3 or higher.
  • Patients with unstable hemodynamics at enrollment.
  • Patients with right coronary artery disease that is chronic total occlusion and difficult to treat with PCI (J-CTO score of ≥ 23).
  • Patients receiving long-term dialysis.
  • Patients who are allergic to antiplatelet agent.
  • Patients who are critically allergic to contrast media.
  • Patients who are allergic to any DES component.

结局指标

主要结局

Major adverse cardiovascular event (death, myocardial infarction, cerebrovascular disorder, and repeat revascularization)

时间窗: 12 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ken Kozuma

Professor

Teikyo University

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