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OpenTrials
Completed

NCT Number: NCT02945748

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

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.

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Key information

Age range

2 day–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Schneider's children medical center

Petah Tikva, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Raise>10% in cardiac index following therapy

    Time frame: 20 minutes

Sponsors and collaborators

Lead sponsor

Rabin Medical Center

Other

Registry information

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Oct 26, 2016
Registry last updated
Mar 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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