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Performance for French Pediatric Intensive Care Units

Creation of a Composite Indicator of Clinical and Economic Performance for French Pediatric Intensive Care Units

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05491018
Acronym
QUAL-REAPED
Enrollment
13270
Registered
2022-08-08
Start date
2027-01-01
Completion date
2027-10-01
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severity of Illness Index

Keywords

Pediatric, intensive care, Severity of Illness, economic, scoring system

Brief summary

Introduction. The measurement of severity scores in adult and pediatric resuscitation provides a tool for evaluating the clinical performance of resuscitation services. No pediatric studies have investigated the association between current procedure and diagnostic cost indices with pediatric ICU patient severity and mortality. Objectives. The main objective of this project in real-life situations, in 14 French pediatric intensive care units, is to validate the recently available PIM3 and PRISM IV severity scores, which take into account the clinical dimension of performance in pediatric intensive care. This project is a French multicenter prospective observational research project involving 14 French pediatric intensive care units belonging to the Groupe Francophone de Réanimation et Urgences Pédiatriques (GFRUP). All patients under 18 years of age admitted to the 14 pediatric intensive care units affiliated with the GFRUP and voluntarily participating in the project will be included in the study. Expected outcomes are: Validation of PIM3 and PRISM IV scores in a French population to assess clinical performance. To develop a predictive model of mortality and a predictive model of cost in French pediatric intensive care units.

Interventions

None listed

Sponsors

University Hospital, Lille
Lead SponsorOTHER
Ministry of Health, France
CollaboratorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* All patients under 18 years of age admitted to the 14 pediatric intensive care units and voluntarily participating in the project will be included in the study.

Exclusion criteria

\- Children of age of reason or parents/legal guardians of children refusing participation in this project will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Survival : yes / noAt PICU discharge,through study completion, an average of 2 years

Secondary

MeasureTime frame
cost of PICU stayAt PICU discharge,through study completion, an average of 2 years

Contacts

CONTACTStéphane Leteurtre, MD,PhD
stephane.leteurtre@chru-lille.fr03 20 44 68 84
PRINCIPAL_INVESTIGATORStéphane Leteurtre, MD,PhD

University Hospital, Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026