CompletedNot Applicable

Uninvasive Cardiac Output Monitoring (USCOM) in Critically Ill Children: Validation and Prediction of Hemodynamic Instability

Israel52 participantsStarted 2016-07

Plain-language summary

Hemodynamically unstable ventilated PICU \& PCICU patients, which a decision for commencement in inotropic therapy or fluid bolus has been made, will be recruited. Hemodynamic measurements will be carried out before and after therapy have been made, including customary hemodynamic parameters, echocardiography and USCOM studies. All parameters will be analyzed for fluid responsiveness or inotropic therapy prediction. Trend in USCOM parameters will be compared to echocardiography CO parameters.

Who can participate

Age range2 Days – 18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Pediatric critically ill ventilated patients admitted to PICU \& PCICU * Hemodynamically unstable which a decision for commencement in inotropic therapy or fluid bolus has been made * parental concent Exclusion Criteria: * Cardiac shunt * Aortal anomaly \\ Repair * Tracheostomy * Parental refusal to participate

What they're measuring

Raise>10% in cardiac index following therapy

Timeframe: 20 minutes

Trial details

NCT IDNCT02945748

SponsorRabin Medical Center

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-08

View on ClinicalTrials.gov More Hemodynamic Instability trials