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Nasal Humidified High Flow Oxygen During Weaning From Mechanical Ventilation : Ultrasonography Study

Not Applicable
Completed
Conditions
Consent of Patients
Arterial Line
Adult Patients Ventilated More Than 48 h
Stable 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
GroupInterventionDescription
optiflowmechanical ventilation-
O2mechanical ventilation-
Primary Outcome Measures
NameTimeMethod
variations of lung ultrasound score24 hours after extubation
Secondary Outcome Measures
NameTimeMethod
Lung ultrasound scoreat baseline, 4-6 hours after extubation, 24 hours after extubation, 48 hours after extubation
rates of patients with postextubation distressduring the 48th post-extubation
Electrical Impedance tomographyat baseline, 4-6 hours after extubation, 24 hours after extubation, 48 hours after extubation
Epithelial and endothelial biomarkersat 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

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