Skip to main content
Clinical Trials/NCT06146439
NCT06146439
Completed
Not Applicable

Determination of the Factors Causing Treatment Failure in Children Receiving Oxygen Therapy With High-flow Nasal Cannula Due to Moderate and Severe Respiratory Distress

Dr. Behcet Uz Children's Hospital1 site in 1 country201 target enrollmentOctober 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
High-flow Nasal Cannula
Sponsor
Dr. Behcet Uz Children's Hospital
Enrollment
201
Locations
1
Primary Endpoint
HFNC treatment outcome (failure or success)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this observational study is to identify the variables that predict treatment failure in order to identify the patients in which HFNC treatment may fail and not delay the transition to advanced respiratory support treatments in these patients.

The main questions it aims to answer are:

  • What factors contribute to the failure of HFNC treatment in these children?
  • What is the frequency of HFNC treatment failure in children with moderate and severe respiratory distress? Researchers will compare the group whose HFNC treatment was successful with the group whose HFNC treatment failed to identify factors that cause treatment failure.

Detailed Description

Oxygen therapy with a high-flow nasal cannula (HFNC) is a well-tolerated, relatively new, non-invasive alternative ventilation treatment modality. On the other hand, HFNC failure delays advanced respirator supportive treatments, prolongs hospitalization in the intensive care unit, and emergency department, and causes a significant increase in morbidity and mortality with hypoxemia, neurological impairment, and/or hemodynamic instability. The investigators aimed to identify the variables that predict treatment failure in order to identify the patients in which HFNC treatment may fail and not delay the transition to advanced respiratory support treatments in these patients.

Registry
clinicaltrials.gov
Start Date
October 1, 2018
End Date
February 1, 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Dr. Behcet Uz Children's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Derşan Onur

Principal Investigator

Dr. Behcet Uz Children's Hospital

Eligibility Criteria

Inclusion Criteria

  • Moderate to severe respiratory distress
  • Oxygen therapy with high-flow nasal cannula

Exclusion Criteria

  • Chronic lung disease (those with CO2 retention or hypoxia in their daily life)
  • Cyanotic congenital heart disease
  • Craniofacial malformation
  • Trauma patients
  • Hypotonic patients
  • Cases with tracheostomy
  • Patients using HFNC therapy for respiratory support after extubation

Outcomes

Primary Outcomes

HFNC treatment outcome (failure or success)

Time Frame: 30 days

Whether advanced respiratory support treatments (invasive and noninvasive mechanical ventilation) are needed

Study Sites (1)

Loading locations...

Similar Trials