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Clinical Trials/NCT05491018
NCT05491018Not yet recruitingNot Applicable

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

University Hospital, Lille0 sites13,270 target enrollmentStarted: January 1, 2027Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
13,270
Primary Endpoint
Survival : yes / no

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
— to 18 Years (Child, Adult)
Sex
All
Accepts 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.

Outcomes

Primary Outcomes

Survival : yes / no

Time Frame: At PICU discharge,through study completion, an average of 2 years

Secondary Outcomes

  • cost of PICU stay(At PICU discharge,through study completion, an average of 2 years)

Investigators

Sponsor
University Hospital, Lille
Sponsor Class
Other
Responsible Party
Sponsor

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