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Not yet recruiting NCT06470932

Outcome of Patients Admitted to Pediatric Intensive Care for Acute Respiratory Failure

No phase Interventional Pediatric Respiratory Diseases

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Follow-up consult.
Who it may be relevant to
Registry conditions: Pediatric Respiratory Diseases. Basic parameters: 2 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This study aims to assess the quality of life of patients six months after admission to a pediatric intensive care unit for acute respiratory failure. Children's quality of life will be assessed using the PedsQL scale at 6 months. This is a prospective cohort diagnostic and prognostic study.

Interventions

  • Diagnostic test Follow-up consult
    Patients will be ask to participate to a follow-up consult

Primary outcome measures

  • Quality of life at 3 months [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • admitted in the PICU of Grenoble-Alps University Hospital
  • for acute respiratory failure (code J960) requiring mechanical ventilation for at least 48hrs

Exclusion criteria

  • already followed-up by a pediatric pulmonologist
  • with congenital disease
  • with long term ventilation
  • still admitted at 3 months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06470932 · 38RC23.0449

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗