- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02186288
Effect of High-flow Nasal Cannula Oxygen on Lung Volumes Determined by Electrical Impedance Tomography (OXIDIA)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Prospective clinical study in ICU with patients requiring High-flow nasal cannula oxygen comparing lung volumes determined by electrical impedance tomography and diaphragmatic ultrasound before, during and after High-flow nasal cannula oxygen.
Duration of High-flow nasal cannula oxygen is 30 minutes.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Clermont-Ferrand, France, 63003
- CHU Clermont-Ferrand
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
• Adult ICU patients requiring High-flow nasal cannula oxygen
- Consent of patients or family
- Arterial line
Exclusion Criteria:
• Tracheotomized patients
- Dressings in the thoracic area
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Adult ICU patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
End-expiratory lung volume (EELV) determined by electrical impedance tomography before NIV non invasive ventilation
Time Frame: at day 1
|
at day 1
|
End-expiratory lung volume (EELV) determined by electrical impedance tomography during NIV non invasive ventilation
Time Frame: at day 1
|
at day 1
|
End-expiratory lung volume (EELV) determined by electrical impedance tomography after NIV non invasive ventilation
Time Frame: at day 1
|
at day 1
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Anterior, medio-anterior, medio-posterior and posterior EELV at each time
Time Frame: at day 1
|
at day 1
|
Diaphragmatic excursion and thickness determined by ultrasound
Time Frame: at day 1
|
at day 1
|
Ventilatory frequency
Time Frame: at day 1
|
at day 1
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CHU-0196
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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