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临床试验/NL-OMON43561
NL-OMON43561已完成3 期

Pre-emptive, OCT guided angioplasty of vulnerable, intermediate coronary lesions: a randomized trial - the PECTUS trial

Vrije Universiteit Medisch Centrum0 个研究点目标入组 1,000 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
1,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - patients with acute myocardial infarction and residual, non-obstructive CAD, with the possibility of plaque vulnerability.
  • - the coronary lesion must be suitable for PCI with a commercially available BVS.

排除标准

  • - Refusal or inability to provide informed consent.
  • - < 18 years of age
  • - Previous CABG.
  • - Indication for revascularization by CABG.
  • - Target vessel diameter < 2,5 mm or >4.0 mm
  • - Anatomy or lesions unsuitable for OCT catheter crossing or imaging (aorta-ostial lesions, small diameter segment, severe calcifications)
  • - Anatomy unsuitable for BVS placement (left main, bifurcation stenting, sidebranch (> 2 mm) involvement).
  • - Target lesion is instent restenosis
  • - Target lesion is chronic total occlusion
  • - Severe kidney disease defined as an eGFR < 30 ml/min.
  • - Target lesion in the same vessel as the treated culprit lesion
  • - Target lesion in the same segment as a previously implanted stent/scaffold
  • - Estimated life expectancy < 1 year

研究者

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