跳至主要内容
临床试验/ISRCTN21662248
ISRCTN21662248已完成未知

A randomised, comparative effectiveness study of COMPLETE versus culprit-only revascularization strategies to treat multi-vessel disease after primary percutaneous coronary interventions (PCI) for ST-segment elevation myocardial infarction

Population Health Research Institute (Canada)0 个研究点目标入组 4,041 人开始时间: 2014年1月16日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
4,041

研究概览

简要总结

2019 results in https://pubmed.ncbi.nlm.nih.gov/31475795/ (added 14/04/2021)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Men and women within 72 hours after successful PCI (preferably using a drug-eluting stent) to the culprit lesion for STEMI. PCI for STEMI can be either primary PCI or rescue PCI for failed fibrinolysis or a pharmacoinvasive strategy where PCI is performed routinely 3-12 hours after initiation of fibrinolysis
  • 2. Multi-vessel disease defined as at least 1 additional non-infarct related coronary artery lesion that is at least 2.5 mm in diameter that has not been stented as part of the primary PCI and that is amenable to successful treatment with PCI and has
  • 2.1. at least 70% diameter stenosis (visual estimation) or
  • 2.1. at least 50% diameter stenosis (visual estimation) with fractional flow reserve less than or equal to 0.80

排除标准

  • 1. Planned revascularisation of non-culprit lesion(s)
  • 2. Planned surgical revascularisation
  • 3. Non-cardiovascular co-morbidity reducing life expectancy to less than 5 years
  • 4. Any factor precluding 5 year follow up.
  • 5. Prior coronary artery bypass graft (CABG) surgery.

研究者

发起方
Population Health Research Institute (Canada)

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