High Flow Nasal Cannula in Pediatric Patients After Cardiothoracic Surgery
NCT04451057 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 286
Last updated 2024-07-08
Summary
High flow nasal cannula(HFNC) ventilation can provide such effects as wash-out effect of the carbon dioxide inside the anatomical dead space,some level of continuous airway pressure and humidified oxygen gases.
Therefore because of its physiological benefits, it has been reported that HFNC can reduce "treatment failure" after extubation in pediatric patients like preterm babies,or infants who suffer from bronchitis.
However there is no evidence showing that HFNC can reduce "treatment failure" after extubation in pediatric patients after cardiothoracic surgery.
This multi-center randomized controlled trial (RCT) involving pediatric patients after cardiothoracic surgery will be conducted to determine whether HFNC,compared with conventional oxygen therapy,after extubation can reduce the rate of"escalation of care due to treatment failure".
Conditions
- Pediatric Patients After Cardiothoracic Surgery
Interventions
- DEVICE
-
high flow nasal cannula therapy
Once extubation has taken place, the child will be placed either on conventional oxygen therapy or high flow nasal cannulae according to randomization
- DEVICE
-
low flow nasal cannula therapy
Once extubation has taken place, the child will be placed either on conventional oxygen therapy or high flow nasal cannulae according to randomization
Sponsors & Collaborators
-
Osaka Women's and Children's Hospital
collaborator UNKNOWN -
Hyogo Prefectural Kobe Children's Hospital
collaborator OTHER -
Osaka City General Hospital
collaborator OTHER -
Aichi Children's Health and Medical Center
collaborator UNKNOWN -
National Center for Child Health and Development
collaborator UNKNOWN -
Osaka University
lead OTHER
Principal Investigators
-
Takeshi Yoshida, MDPhD · Department of Anesthesiology and Intensive Care Medicine, Osaka University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Max Age
- 2 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-08-11
- Primary Completion
- 2024-02-20
- Completion
- 2024-06-30
Countries
- Japan
Study Locations
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