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High Flow Nasal Oxygen Therapy an Implementation Study in Pediatric Wards (HFNO)

E

Epicentre

Status

Not yet enrolling

Conditions

Severe Respiratory Distress
Moderate Respiratory Distress

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06715423
G2429-HFNO_ProcessEvaluation

Details and patient eligibility

About

The purpose of this study is to prospectively evaluate the process of implementing HFNO in several MSF projects, varying according to geographical and programmatic contexts, population, health structures, human resources, and management. It will generate evidence on the operational feasibility (in terms of human resources, equipment, logistics and costs) of integrating HFNO into PICU standard of care, as well as on the users' and caregivers' perspectives on HFNO and on the children clinical outcomes observed where HFNO is implemented. This relevant information will guide MSF in the decision making of scaling up HFNO therapy in its projects.

Full description

Mixed method study: quantitative component for the data of the children and qualitative data for the perception for health staffs and parents

Enrollment

960 estimated patients

Sex

All

Ages

1 month to 5 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • prescription of HFNO by clinician
  • parent consenting to the use of the data

Trial design

960 participants in 1 patient group

Pediactric ICU Hospitalized children 1mo to 5 yo
Description:
Prescription of HFNO therapy

Trial contacts and locations

1

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Central trial contact

Elisabeth Poulet, MD, Msc

Data sourced from clinicaltrials.gov

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