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Performance for French Pediatric Intensive Care Units (QUAL-REAPED)

U

University Hospital, Lille

Status

Not yet enrolling

Conditions

Severity of Illness Index

Study type

Observational

Funder types

Other

Identifiers

NCT05491018
PREPS-18-0433 (Other Identifier)
2018_98

Details and patient eligibility

About

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.

Enrollment

13,270 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

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Central trial contact

Stéphane Leteurtre, MD,PhD

Data sourced from clinicaltrials.gov

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