Routine Microcirculation Measurements in Intensive Care Unit Patients and Validation by PiCCO Technology.ROUMI-study
- Conditions
- Patients with any type of shock in the IC
- Registration Number
- NL-OMON23604
- Lead Sponsor
- Investigator initiated
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
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
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.
oMoribund
oIntra-cardiac shunts, aortic aneurysm, aortic stenosis, mitral or tricuspid insufficiency,
oPneumonectomy, macro lung embolism
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method oTo investigate the correlation of microcirculatory parameter MFI measured with Cytocam-IDF with Cardiac Index measured using the trans-pulmonary hemodilution technique PiCCO
- Secondary Outcome Measures
Name Time Method oTo investigate the value and feasibility of routine monitoring of sublingual microcirculation as an early warning of clinical deterioration/improvement before the diagnosis can be made with laboratory, vital and hemodynamic parameters in critically ill patients.