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临床试验/NL-OMON45423
NL-OMON45423已完成不适用

Physiology and Imaging Pre- and Post Stenting 2 - PIPPS 2

Catharina-ziekenhuis0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • In this study, patients from 18 years are eligible for inclusion if they are scheduled for PCI. De-novo lesions in a 3,0-3,5 mm artery up to 25mm are suitable to be treated.
  • All patients have to be able to give written informed consent.

排除标准

  • - patients < 18 years
  • - Cardiogenic shock
  • - severe calcification or chronic occluded artery.
  • - bifurcation lesions
  • - previous bypass surgery
  • - pregnancy
  • - inability to give informed consent
  • - contra-indication for adenosine infusion such as allergy.

研究者

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Physiology and Imaging Pre- and Post Stenting 2 | 临床试验