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Clinical Trials/ACTRN12618000210279
ACTRN12618000210279
Completed
Phase 3

asal High Flow therapy versus standard oxygen delivery for Children with Acute Hypoxemic Respiratory Failure - a Randomised Controlled Trial to evaluate hospital length of stay and treatment failure.

Paediatric Critical Care Research Group0 sites1,512 target enrollmentFebruary 9, 2018

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Acute respiratory failure
Sponsor
Paediatric Critical Care Research Group
Enrollment
1512
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 9, 2018
End Date
March 27, 2020
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Paediatric Critical Care Research Group

Eligibility Criteria

Inclusion Criteria

  • Children aged 1\-4 years of age (up to but excluding 5th birthday) with the clinical diagnosis of an Acute Hypoxemic Respiratory Failure disease process such as acute lower respiratory tract infection or asthma, or pnuemonia as examples, and an oxygen requirement in room air (SpO2 \<90/92%)
  • Included are infants with reactive airway disease \>12 months and an oxygen requirement in room air (SpO2 \<90/92%). This includes infants \>12 months with the diagnosis of bronchiolitis
  • Informed consent from parents or guardians

Exclusion Criteria

  • Oxygen requirement and therapy in the emergency department existed for longer than 4 hours prior to inclusion (excludes oxygen given in ambulance or other hospital)
  • Previous use of NHF therapy
  • Upper airway obstruction
  • Craniofacial malformations
  • Critically ill infants requiring immediate higher level of respiratory support i.e. NIV or invasive ventilation, low level of consciousness.
  • Basal skull fracture
  • Cyanotic Heart Disease
  • Home Oxygen therapy
  • Apnoeas (defined as requiring respiratory support such as NIV or mechanical ventilation)
  • Cystic Fibrosis

Outcomes

Primary Outcomes

Not specified

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