跳至主要内容
临床试验/NL-OMON23604
NL-OMON23604招募中不适用

Comparison and Validation of Cytocam-IDF imaging with PiCCO technology.

Investigator initiated0 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
招募中
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
Observational

入排标准

入选标准

  • •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
  • •oSigned informed consent from the patient or his/her legal representative
  • •oBe suitable for monitoring in the intensive care unit
  • •oShould be older than 18 years
  • •oEligible for sublingual microcirculatory evaluation (not to have maxillofacial injury, bleeding in the mouth)
  • •oShould be under PiCCO monitorization with routine clinic indication

排除标准

  • •o<18 years old
  • •oWoman of childbearing potential with a positive pregnancy test
  • •oRefusal to participate in the study or demand to end study for any reason
  • •oResistance during the measurements of sublingual microcirculation will lead to end of the study.
  • •oIntra-cardiac shunts, aortic aneurysm, aortic stenosis, mitral or tricuspid insufficiency,
  • •oPneumonectomy, macro lung embolism

研究者

发起方
Investigator initiated

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