Clinical Trials Directory

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UnknownNCT04451057

High Flow Nasal Cannula in Pediatric Patients After Cardiothoracic Surgery

High Flow Nasal Cannula in Pediatric Patients After Cardiothoracic Surgery:A Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
286 (estimated)
Sponsor
Osaka University · Academic / Other
Sex
All
Age
2 Years
Healthy volunteers
Not accepted

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".

Detailed description

The multi-center RCT will enroll 380 pediatric patients after cardiothoracic surgery from the Intensive Care Units (ICUs) in Japan.Informed consent will be obtained from the their parents or legally representatives.They will receive postoperative standard care in ICU and spontaneous breathing test(SBT).If SBT will be done successfully,they will be extubated.Just before extubation,they will be divided randomly into the intervention group or the control group.After randomization,they will be extubated.After extubation,the intervention group will receive HFNC therapy,while the control group will receive conventional oxygen therapy.The flow in the intervention group will surely be maintained to be high,while the flow in control group will surely be less than 2 liter/min.In both groups,outcome measure will be assessed within 72 hours after extubation,or during ICU stay.

Conditions

Interventions

TypeNameDescription
DEVICEhigh flow nasal cannula therapyOnce extubation has taken place, the child will be placed either on conventional oxygen therapy or high flow nasal cannulae according to randomization
DEVICElow flow nasal cannula therapyOnce extubation has taken place, the child will be placed either on conventional oxygen therapy or high flow nasal cannulae according to randomization

Timeline

Start date
2020-08-11
Primary completion
2024-02-20
Completion
2024-06-30
First posted
2020-06-30
Last updated
2024-07-08

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT04451057. Inclusion in this directory is not an endorsement.