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Clinical Trials/NL-OMON49817
NL-OMON49817
Recruiting
N/A

Routine Microcirculation Measurements in Intensive Care Unit Patients and Validation by PiCCO Technology. ROUMI-study - Comparison and Validation of Cytocam-IDF imaging with PiCCO technology.

HagaZiekenhuis0 sites30 target enrollmentTBD
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Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
HagaZiekenhuis
Enrollment
30
Status
Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •o Should be under PiCCO monitorization with routine clinic indication
  • •o Should be older than 18 years
  • •o Be suitable for monitoring in the intensive care unit
  • •o Eligible for sublingual microcirculatory evaluation (not to have
  • •maxillofacial injury, bleeding in the mouth)

Exclusion Criteria

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

Outcomes

Primary Outcomes

Not specified

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