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Recruiting NCT07383051

A Randomized Clinical Trial for Predictors of Successful Extubation of Pediatric Patients With or Without High Velocity Nasal Insufflation

No phase Interventional High Velocity Nasal Insufflation Simple Oxygen Weaning Criteria

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: Comparing the outcome of pediatric patients after successful weaning on either High Velocity Nasal Insufflation or simple oxygen, comparing High Velocity Nasal Insufflation to simple oxygen after successful weaning of pediatric patients.
Who it may be relevant to
Registry conditions: High Velocity Nasal Insufflation, Simple Oxygen, Weaning Criteria. Basic parameters: 2 months — 13 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
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Predictors of Successful Extubation of Pediatric Patients From Mechanical Ventilation With or Without Post Extubation High Velocity Nasal Insufflation

Overview

A randomized clinical trial about predictors of successful extubation of pediatric patients from mechanical ventilation either on High Velocity Nasal Insufflation or simple nasal oxygen and comparing the outcome

Detailed description

A randomized clinical study is comparing between extubation on High Velocity Nasal Insufflation or simple nasal Oxygen ensuring that all patients had successful weaning predictors before extubation and comparing the outcome whether patient needed upgrading of oxygen support or re-intubation within 48 hours, presence of respiratory distress or stridor post extubation, time of complete weaning of oxygen support to room air and also morbidity and mortality.

Interventions

  • Device Comparing the outcome of pediatric patients after successful weaning on either High Velocity Nasal Insufflation or simple oxygen
    A randomized clinical study is comparing between extubation on High Velocity Nasal Insufflation or simple nasal Oxygen ensuring that all patients had successful weaning predictors before extubation and comparing the outcome whether patient needed upgrading of oxygen support or re-intubation within 48 hours, presence of respiratory distress or stridor post extubation, time of complete weaning of oxygen support to room air and also morbidity and mortality.
  • Device comparing High Velocity Nasal Insufflation to simple oxygen after successful weaning of pediatric patients
    A randomized clinical study is comparing between extubation on High Velocity Nasal Insufflation or simple nasal Oxygen ensuring that all patients had successful weaning predictors before extubation and comparing the outcome whether patient needed upgrading of oxygen support or re-intubation within 48 hours, presence of respiratory distress or stridor post extubation, time of complete weaning of oxygen support to room air and also morbidity and mortality.

Primary outcome measures

  • comparing the need for reintubation within 48 hours afterr extubation using High Velocity Nasal Insufflation versus simple oxygen [Time frame: 48 hours]

Eligibility criteria

Inclusion criteria

  • Age between 2 months and 13 years old with minimum weight 4kg
  • Both sexes
  • Patients on mechanical ventilation for at least 24 hours for any indication

Exclusion criteria

  • Patients not ready for weaning from mechanical ventilation
  • Contraindications to use of High velocity nasal insufflation
  • Prolonged mechanical ventilation for more than 21 days

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

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Supportive care

Study locations

Egypt · 1 center
  • Cairo University — Cairo

Identifiers

NCT: NCT07383051 · MD-299-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗