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COMPLETED
NCT02824744
NA

Comparison Between 2l vs 3l in HFNC During the Initial Management of Severe Bronchiolitis in Infants

Sponsor: University Hospital, Montpellier

View on ClinicalTrials.gov

Summary

The purpose of the study is to evaluate prospectively the clinical benefits of 2 different flow with High flow nasal canula (HFNC: 2l/kg/min) versus (HFNC: 2l/kg/min) in the initial management of bronchiolitis in infants. Design: Prospective, controlled, randomized, multi-center. Design: Infants less than 6 month admitted in pediatric intensive care unit for respiratory distress (mWCAS \>3) secondary to bronchiolitis but not requiring mechanical ventilation will be randomized in two groups:HFNC "2l/min/kg" or HFNC "3l/min/kg" during 24 hours. Conditions of measurements: Primary endpoint: Proportion of failure in both arms during the first 24 hours. Failure criteria: A raise of the Clinical score for respiratory distress (mWCAS) (1 point) or respiratory rate (10/min /H0 and above 60/min) or discomfort (EDIN) (1point /H0 and above 4) or apnea. Secondary outcomes: Assessment at H1, H12, H24 of mWCAS, respiratory and heart rate, EDIN score, skin lesions, FiO2 required to achieve an oxygen saturation between 94 and 97%, transcutaneous PCO2 (correlated to an initial gas analysis), Report SpO2 / FiO2 Statistic: Intention to treat Analysis. Expected number of patients: 135 per arm: 270 children.

Official title: Comparison Between 2l/Min/kg vs 3l/Min/kg in High Flow Nasal Cannula (HFNC) During the Initial Management of Severe Bronchiolitis in Infants

Key Details

Gender

All

Age Range

0 Hours - 6 Months

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2016-11-02

Completion Date

2018-03

Last Updated

2026-06-15

Healthy Volunteers

No

Conditions

Interventions

DEVICE

treatment by 2l/min/kg in High Flow Nasal cannula (HFNC)

DEVICE

treatment by 3l/min/kg in High Flow Nasal cannula (HFNC)

Locations (1)

University hospital of Montpellier

Montpellier, France