NCT07099664 Use of the Aortic Time-velocity Integral Via Suprasternal Ultrasound to Search Preload Dependence in Paediatric Surgery : Kid's Fluid Management (FM)
| NCT ID | NCT07099664 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University Hospital, Lille |
| Condition | Hemodynamic |
| Study Type | OBSERVATIONAL |
| Enrollment | 90 participants |
| Start Date | 2025-10-03 |
| Primary Completion | 2026-08 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 90 participants in total. It began in 2025-10-03 with a primary completion date of 2026-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
After major surgery, fluid overload is associated with an increase of morbidity and mortality. Fluid administration should therefore be given wisely. However, there is a paucity of monitor to predict preload dependence in paediatric anaesthesia. The aim of this study is to determine if VTI variation, measured through the suprasternal window, with a cardiac doppler probe, can predict preload dependence. Indeed, cardiac probe are present in most operating room and suprasternal window is reachable in most surgical case, which should allow VTI monitoring for the vast majority of our patient.
Eligibility Criteria
Inclusion Criteria: * Patient under 18 admitted to paediatric operating room for a surgical intervention, an endoscopy, an interventional radiology procedure or an imagery and needing a general anaesthesia. Exclusion Criteria: * Condition preventing a suprasternal ultrasound (tracheostomy, spinal immobilization, suprasternal bandage) * Pathology disturbing respiratory variation of left ventricular stroke volume (PAH, constrictive pericarditis, pericardial effusion, right ventricular dysfunction, complex congenital heart disease, aortic coarctation, patent ductus arteriosus * Every medical condition where Berry's rule of fasting compensation could be unsafe (anuric kidney failure, oedema, heart failure with reduce left ventricular ejection fraction, patient under vasoactive drugs * Opposition to the participation in the study * Pregnant women * Patient with no security coverage * Inability to determine baseline cardiac output
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07099664 clinical trial?
This trial is open to participants of all sexes, aged 0 Years or older, up to 18 Years, studying Hemodynamic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07099664 currently recruiting?
Yes, NCT07099664 is actively recruiting participants. Contact the research team at Martin.DUBERNET@chu-lille.fr for enrollment information.
Where is the NCT07099664 trial being conducted?
This trial is being conducted at Lille, France.
Who is sponsoring the NCT07099664 clinical trial?
NCT07099664 is sponsored by University Hospital, Lille. The trial plans to enroll 90 participants.