Routine Microcirculation Measurements in Intensive Care Unit Patients and Validation by PiCCO Technology. ROUMI-study
- Conditions
- 10019280BloedsomloopCirculationorgan perfusion
- Registration Number
- NL-OMON49817
- Lead Sponsor
- HagaZiekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
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)
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 Moribund
o Intra-cardiac shunts, aortic aneurysm, aortic stenosis, mitral or tricuspid
insufficiency,
o Pneumonectomy, macro lung embolism
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>2.1 Primary Objectives:<br /><br>o To investigate the correlation of microcirculatory parameter MFI measured<br /><br>with Cytocam-IDF with Cardiac Index measured using the trans-pulmonary<br /><br>hemodilution technique PiCCO.<br /><br>o To assess the association between the microcirculatory parameters and<br /><br>macro-hemodynamic parameters during admission and interventions such as fluid<br /><br>resuscitation and vasopressor/inotrope/vasodilator administration.</p><br>
- Secondary Outcome Measures
Name Time Method