Nasal Humidified High Flow Oxygen During Weaning From Mechanical Ventilation : Ultrasonography Study
Not Applicable
Completed
- Conditions
- Consent of PatientsArterial LineAdult Patients Ventilated More Than 48 hStable Respiratory and Hemodynamic Conditions for SBT
- Interventions
- Other: mechanical ventilation
- Registration Number
- NCT01702779
- Lead Sponsor
- University Hospital, Clermont-Ferrand
- Brief Summary
This is a prospective, randomized clinical multicentric study in ICU (Intensive Care University)during weaning from mechanical ventilation.
- Detailed Description
Prospective randomized clinical multicentric study on ICU (Intensive Care University) comparing nasal humidified high flow therapy versus standard oxygen with Lung Ultrasound Score during weaning from mechanical ventilation
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
- Adult patients ventilated more than 48 h
- Stable respiratory and hemodynamic conditions for SBT
- Consent of patients
- Arterial line
Exclusion Criteria
- COBP
- Laryngeal dyspnea
- Tracheostomy
- Arythmya
- No echogenicity
- Paraplegia >T8
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description optiflow mechanical ventilation - O2 mechanical ventilation -
- Primary Outcome Measures
Name Time Method variations of lung ultrasound score 24 hours after extubation
- Secondary Outcome Measures
Name Time Method Lung ultrasound score at baseline, 4-6 hours after extubation, 24 hours after extubation, 48 hours after extubation rates of patients with postextubation distress during the 48th post-extubation Electrical Impedance tomography at baseline, 4-6 hours after extubation, 24 hours after extubation, 48 hours after extubation Epithelial and endothelial biomarkers at baseline, 4-6 hours after extubation, 24 hours after extubation, 48 hours after extubation
Trial Locations
- Locations (1)
CHU Clermont-Ferrand
馃嚝馃嚪Clermont-Ferrand, France