跳至主要内容
临床试验/NL-OMON35057
NL-OMON35057已完成不适用

RAndomized comParison between the Stentys self-exPanding COronary Stent and a balloon-expandable stent In AcuTe MyocardIal InfarctiON - APPOSITION II

Stentys0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Stentys
入组人数
40

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
18 至 99(—)

入选标准

  • Subjects presenting with acute myocardial infarction with a de novo stenotic lesion in a native coronary artery amenable to revascularization with percutaneous coronary intervention with stent deployment.;Inclusion criteria
  • 1.Subject >=18 years old.
  • 2. Myocardial infarction
  • 3. candidate for CABG
  • 4. Patient understands nature of research and is willing to comply to follow-up investigations
  • 5. vessel diameter is between 2.5 and 4.0 mm and length is < 30mm

排除标准

  • 1. Currently enrolled in another investigational study
  • 2. Coronary or cardiac intervention or major surgery of any kind within 30 days prior to the procedure.
  • 3. Patients on anticoagulation therapy (Coumadin)
  • 4. Cardiogenic shock
  • 5. Co-morbid condition(s) that could limit the subject's ability to participate in the study or to comply with follow-up requirements, or impact the scientific integrity of the study.
  • 6. Cerebrovascular accident or transient ischemic attack in the last 6 months.
  • 7. Known hypersensitivity or contraindication to aspirin, heparin or bivalirudin, clopidogrel or ticlopidine, cobalt, nickel, or sensitivity to contrast media, which cannot be adequately pre-medicated.
  • 8. Known serum creatinine level >2.5mg/dl or presence or history of renal failure
  • 9. Target lesion is severely calcified.

研究者

发起方
Stentys

相似试验