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临床试验/NCT01124890
NCT01124890已完成4 期

Southwest German Interventional Study in Acute Myocardial Infarction III

University Hospital, Saarland2 个研究点 分布在 1 个国家目标入组 197 人开始时间: 1998年7月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
197
试验地点
2
主要终点
Major Adverse Cardiovascular Events

研究概览

简要总结

SIAM III was a multicenter, randomized, prospective, controlled trial in patients with ST-elevation myocardial infarction receiving fibrinolysis <12 hours after onset of symptoms. Patients of the early PCI group were transferred within 6 hours after fibrinolysis for PCI. The conservative group received elective PCI two weeks after fibrinolysis.

详细描述

SIAM III was a multicenter, randomized, prospective, controlled trial in patients with ST-elevation myocardial infarction receiving fibrinolysis <12 hours after onset of symptoms. All patients received reteplase, aspirin in combination with ticlopidin, and heparin. Patients of the early PCI group were transferred within 6 hours after fibrinolysis for PCI. The conservative group received elective PCI two weeks after fibrinolysis. In total 197 patients were included, 163 were treated by PCI. The primary end point was the composite of ischemic events, death, reinfarction, and target lesion revascularization.

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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptoms of MI present for 12 h
  • ST segment elevation of at least 1 mm in two or more limb leads,
  • ST segment elevation of at least 2 mm in the precordial leads,
  • or new bundlebranch block
  • Patients eligible for thrombolysis
  • Informed consent for participation

排除标准

  • Secondary or iatrogenic infarction
  • Chronic renal insufficiency requiring dialysis
  • Coronary anatomy unsuitable for stent placement
  • Anticipated indication for surgical coronary revascularization within 6 months
  • Previous MI in the area of the infarct related vessel
  • Infarct related lesion not clearly defined

结局指标

主要结局

Major Adverse Cardiovascular Events

时间窗: 6 months

The primary endpoint was a combined endpoint consisting of death, reinfarction, ischemic events, and target vessel revascularization.

次要结局

  • Reinfarction(6 months)
  • Ischemic Events(6 months)
  • Target Vessel Revascularization(6 months)
  • Death(6 months)

研究者

发起方
University Hospital, Saarland
申办方类型
Other
责任方
Sponsor

研究点 (2)

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