22
Participants
Start Date
September 16, 2021
Primary Completion Date
April 24, 2024
Study Completion Date
April 24, 2024
Non-invasive ventilation (NIV)
Non-invasive ventilation will be provided through a mechanical ventilator (Carina, Dräger) through a facial interface (Fitlife Respironics, Philips). A PEEP level between 5 and 10 cmH2O, minimal pressure-support level of 5 cm H2O targeting a tidal volume around 6 to 8 ml/kg and at the same FiO2 applied during the spontaneous breathing trial.
High-flow nasal cannula
High flow nasal cannula will be provided through a commercial device (AIRVO2 + Optiflow nasal cannula, Fisher \& Paykel), at 50 LPM and at the same FiO2 applied during the spontaneous breathing trial.
Hospital Clínico UC Christus, Santiago
Fondo Nacional de Desarrollo Científico y Tecnológico, Chile
OTHER_GOV
Pontificia Universidad Catolica de Chile
OTHER