跳至主要内容
临床试验/NCT01435408
NCT01435408进行中(未招募)不适用

A Randomised Comparison of the Clinical Outcome After Postconditioning or Deferred Stent Implantation Versus Conventional Treatment

Rigshospitalet, Denmark10 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
2,000
试验地点
10
主要终点
All cause mortality, heart failure (postconditioning)

研究概览

简要总结

This study focuses on Cardioprotective strategies.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years.
  • Acute onset of chest pain of < 12 hours' duration.
  • ST-segment elevation ≥ 0.1 mV in ≥ 2 contiguous leads, signs of a true posterior infarction or documented newly developed left bundle branch block.
  • Culprit lesion in a major native vessel.

排除标准

  • Pregnancy.
  • Known intolerance of ASA, clopidogrel, heparin or contrast.
  • Inability to understand information or to provide informed consent.
  • Haemorrhagic diathesis or known coagulopathy.
  • Stent thrombosis.

结局指标

主要结局

All cause mortality, heart failure (postconditioning)

时间窗: 2 years

次要结局

  • All cause mortality, myocardial infarction, repeat revascularisation and occurrence of definite stent thrombosis according to ARC definition within 1 year (deferred stent strategy)(1 year)
  • Infarct size in relation to area at risk as determined by MRI after 3 month(3 month)

研究者

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

Thomas Engstrom

MD, DMSci, PhD

Rigshospitalet, Denmark

研究点 (10)

Loading locations...

相似试验