Last updated: December 20, 2023
Sponsor: University of Padova
Overall Status: Completed
Phase
N/A
Condition
N/ATreatment
Symmetrical high flow nasal cannula (HFNO)
Asymmetrical high flow nasal cannula (DUET HFNO)
Clinical Study ID
NCT05838326
AOP2949
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- age >18 years old;
- invasive mechanical ventilation > 24h;
- acute respiratory failure within 120 minutes after extubation (defined during aspontaneous trial using Venturi mask and assessing a PaO2/FiO2 ratio < 300;
- absence of Sars-Cov-2 positivity;
- absence of cardiological or long-term respiratory disease
Exclusion
Exclusion Criteria:
- pregnancy
- tracheostomy
- non-invasive ventilation after extubation
- second tracheal intubation
- contraindications for EIT belt
- facial or nose abnormalities
Study Design
Total Participants: 20
Treatment Group(s): 2
Primary Treatment: Symmetrical high flow nasal cannula (HFNO)
Phase:
Study Start date:
May 08, 2023
Estimated Completion Date:
July 30, 2023
Study Description
Connect with a study center
Institute of Anaesthesia and Intensive Care, Padua University hospital
Padova, 35120
ItalySite Not Available
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