跳至主要内容
临床试验/NL-OMON53934
NL-OMON53934尚未招募不适用

Percutaneous versus surgical VA ECMO insertion: a pilot study to evaluate feasibility and safety - Percutaneous versus surgical VA ECMO

Amsterdam UMC0 个研究点目标入组 30 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
尚未招募
发起方
入组人数
30

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 64(—)

入选标准

  • 1. Age above 18
  • 2. Indication for VA ECMO support (according to international guidelines and as
  • discussed in our multidisciplinary team)
  • 3. (Deferred) informed consent by proxy

排除标准

  • Patients who are not suitable for undergoing VA ECMO support according to our
  • standard of practice. In addition, patients undergoing central cannulation in
  • the operating theatre, are excluded from participation, as well as patients
  • with no peripheral vascular access

研究者

发起方
Amsterdam UMC

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