Measuring cardiac output in pediatric ICU using a non-invasive method
Cardiac Output Measurement in Pediatric Intensive Care Unit by Metabolic Monitor (Fick Method) : Prospective Feasibility Study
This study is testing a new non-invasive way to measure heart output in critically ill children to see if it works better than the usual method.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 28 Days to 17 Years |
| Sex | All |
| Sponsor | University Hospital, Montpellier Academic / other |
| Locations | 1 site (Montpellier) |
| Trial ID | NCT05741918 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the feasibility of measuring cardiac output in pediatric intensive care unit patients using Fick's method, which is a non-invasive technique that allows for continuous monitoring. The study compares this method to the traditional echocardiography, which, while non-invasive, is operator-dependent and does not provide continuous data. By assessing the effectiveness of Fick's method, the trial seeks to improve monitoring capabilities for critically ill children. The study will involve patients under 18 years old who meet specific criteria related to their medical condition.
Who should consider this trial
Good fit: Ideal candidates for this study are pediatric patients under 18 years old who weigh over 10 kg and require intubation and a central venous line.
Not a fit: Patients who are mechanically ventilated with a leak or have poor echogenicity preventing echocardiography may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more reliable and continuous method for monitoring cardiac output in pediatric ICU patients.
How similar studies have performed: While the use of Fick's method is established, this specific application in pediatric ICU settings is novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient under 18 years old * Patient over 10 kg * Patient requiring intubation or intubated with a cuffed tube * Patient requiring a central venous line in superior vena cava territory Exclusion Criteria: * Mechanical ventilation with leak * Bad echogenicity preventing echocardiography * Absence of written informed consent * Patient not affiliated to French Health Insurance or not covered by public health insurance * Patient with a legal protection
Where this trial is running
Montpellier
- UH Montpellier — Montpellier, France (Recruiting)
Study contacts
- Study coordinator: Arthur GAVOTTO, PH-U
- Email: a-gavotto@chu-montpellier.fr
- Phone: +334.67.33.66.09
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.