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Clinical Trials/NL-OMON23604
NL-OMON23604RecruitingNot Applicable

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

Investigator initiated0 sites30 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • •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

Exclusion Criteria

  • •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

Investigators

Sponsor
Investigator initiated

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