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临床试验/NCT01160900
NCT01160900
Unknown
3 期

Phase III Study, Multivessel Percutaneous Treatment During Myocardial Infarction

Azienda Ospedaliera San Camillo Forlanini1 个研究点 分布在 1 个国家目标入组 180 人2010年7月

概览

阶段
3 期
干预措施
未指定
疾病 / 适应症
Myocardial Infarction
发起方
Azienda Ospedaliera San Camillo Forlanini
入组人数
180
试验地点
1
主要终点
death at 30 days
最后更新
15年前

概览

简要总结

Few reports described outcomes of complete compared with infarct related artery (IRA) only revascularization in patients with ST elevation myocardial infarction (STEMI) and multivessel coronary disease (CAD).

The purpose of this study is to determine outcome (death, myocardial infarction, target vessel failure) of 180 consecutive patients with STEMI and multivessel CAD undergoing primary angioplasty.

Before the first angioplasty patients are randomized to 2 different strategies: 1) culprit vessel angioplasty only, 2) staged revascularization.

注册库
clinicaltrials.gov
开始日期
2010年7月
结束日期
2012年7月
最后更新
15年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

入排标准

入选标准

  • myocardial acute infarction
  • prolonged chest pain (\>20 minute) started less \<12 hours before arrive in hospital
  • ST segment elevation of \>1mm in \>2 contiguous leads
  • new left bundle branch block
  • diameter of the coronary suitable of angioplasty \>2mm
  • the patients agrees to the study protocol and provides a written consensus
  • two or more coronary suitable for angioplasty

排除标准

  • refused written consensus
  • hypersensitivity or contraindication to any of the following medications: heparin bivalirudin aspirin prasugrel stainless steel
  • history of bleeding
  • cardiogenic shock (PA \< 90mmHg)
  • chronic total occlusion in the second lesion
  • TIMI Flow \< II in the culprit lesion
  • recent pregnancy
  • history of intra-cerebral major hemorrhagic stroke
  • an elective surgical procedure is planned that would necessitate interruption of thienopyridines during the first six months post enrollment life expectancy \<1 year

结局指标

主要结局

death at 30 days

时间窗: 1 month

stent thrombosis

时间窗: 1 year

target vessel failure

时间窗: 1 year

re-acute myocardial infarction

时间窗: 1 month

次要结局

  • bleeding(1 month)
  • timi frame count(1 day)
  • vascular site access complications(1 month)

研究点 (1)

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