Completed
HiFloLUSNasal Humidified High Flow Oxygen During Weaning From Mechanical Ventilation : Ultrasonography Study
What is being tested
mechanical ventilation
+ mechanical ventilation
Other
Who is being recruted
Over 18 Years
+10 Eligibility Criteria
How is the trial designed
Treatment Study
Interventional
Study Start: August 2011
Summary
Principal SponsorUniversity Hospital, Clermont-Ferrand
Last updated: December 2, 2014
Sourced from a government-validated database.Claim as a partner
Study start date: August 1, 2011
Actual date on which the first participant was enrolled.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
Principal SponsorUniversity Hospital, Clermont-Ferrand
Last updated: December 2, 2014
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
4 inclusion criteria required to participate
Adult patients ventilated more than 48 h
Arterial line
Consent of patients
Stable respiratory and hemodynamic conditions for SBT
6 exclusion criteria prevent from participating
Arythmya
COBP
Laryngeal dyspnea
No echogenicity
Show More Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Group II
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
CompletedOne Study Center