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临床试验/KCT0006914
KCT0006914招募中未知

Comparison of clinical outcomes between non-polymer drug-coated stent versus ultrathin strut biodegradable polymer drug-eluting stent in patients undergoing percutaneous coronary intervention: SMART-CHOICE 4 randomized trial

Samsung Medical Center0 个研究点目标入组 3,000 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
3,000

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)Subject must be at least 19 years of age
  • 2)Subject who is able to understand risks, benefits and treatment alternatives and sign informed consent voluntarily.
  • 3)Patients with at least one lesion with equal or greater than 50% diameter stenosis requiring treatment with drug-eluting stents (DES) in native coronary artery or graft

排除标准

  • 1)Patients unable to provide consent
  • 2)Patients with known intolerance major components of drug-eluting stents
  • 3)Patients who have non-cardiac co-morbid conditions with life expectancy <1 year or that may result in protocol non-compliance (per site investigator’s medical judgment)
  • 4)Pregnant or lactating women
  • 5) patient with hemodynamic instability or psychogenic shock

研究者

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