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NCT07255469Recruiting

Metabolic Fluid Responsiveness in Children

Parameters Associated With Metabolic Response to Volume Expansion in Children Post-operative of Cardiac Surgery

Source: ClinicalTrials.gov · Last updated 1 Dec 2025

Brief summary (registry, in English)

The investigators aim to validate markers of metabolic fluid-responsiveness in children with acute circulatory failure following cardiac surgery. This would allow physicians to identify which patient could benefit the most from fluid expansion, thus avoiding useless and potentially dangerous fluid expansions that could lead to fluid overload. To this end, The investigators will evaluate the diagnostic accuracy of the ratio of central venous to arterial carbon dioxide tension (Pv-aCO2) to arteriovenous oxygen content (CavO2), a simple biological marker of anaerobic metabolism, for the diagnosis of metabolic fluid responsiveness defined as a significant increase in oxygen consumption (VO2) after fluid expansion.

Status (registry)
Recruiting
Study type
Observational
Enrollment
110 (estimated)
First submitted
1 Sept 2025
Start date
21 Mar 2025
Primary completion date
21 Mar 2027
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT07255469

What you commit to

  • Study type: Observational
  • Planned participants: 110
  • From 21 Mar 2025 to the primary completion date, 21 Mar 2027
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Impairment of echocardiographic acoustic window or restless patient making ultrasonography impossible

Age

  • Patient less than 37 weeks' corrected gestational age

Other

  • Hemodynamic instability making the delay necessary for any test dangerous
  • Supine position contraindicated or deleterious
  • Opposition to participate expressed by the patient or by a parent or legal guardian

Who the study is looking for

  • Age less than or equal to 15 years old
  • Hospitalization in a pediatric intensive care unit after cardiac surgery
  • Prescription by the attending physician of a fluid expansion of 10ml/kg
  • Prescription of arterial and venous blood gas before and after the volume expansion to help manage acute circulatory failure
  • Patient implanted with a functioning arterial line
  • Patient implanted with a functioning central venous line in the superior vena cava territory

Age in the registry: 0 days to 15 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hôpital Louis Pradel, Hospices Civils de Lyon
Coordinator of this site? Confirm its status
BronFranceRecruiting
Hôpital Jeanne de Flandre - CHU de Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
Hôpital de la Timone - Assistance Publique - Hôpitaux de Marseille
Coordinator of this site? Confirm its status
MarseilleFranceNot yet recruiting
Hôpital mère-enfant - CHU de Nantes
Coordinator of this site? Confirm its status
NantesFranceRecruiting
Hôpital Necker-Enfants Malades - Assistance Publique - Hôpitaux de Paris
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Hôpital Cardiologique Haut Lévêque - CHU de Bordeaux
Coordinator of this site? Confirm its status
PessacFranceRecruiting
Hôpital Felix Guyon - CHU de la Réunion
Coordinator of this site? Confirm its status
Saint-DenisFranceRecruiting
Hôpital des Enfants - CHU de Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.