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NCT02186288 Clinical Trial

Effect of High-flow Nasal Cannula Oxygen on Lung Volumes Determined by Electrical Impedance Tomography

Critical Care Clinical Trial

— OXIDIA  

Official title:
Effect of High-flow Nasal Cannula Oxygen on Lung Volumes Determined by Electrical Impedance Tomography

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02186288
Other study ID # CHU-0196
Secondary ID
Status Completed
Phase N/A
First received June 20, 2014
Last updated July 23, 2015
Start date July 2014
Est. completion date October 2014

Study information
Verified date July 2015
Source University Hospital, Clermont-Ferrand
Contact n/a
Is FDA regulated No
Health authority France: The Commission nationale de l’informatique et des libertés
Study type Observational

Clinical Trial Summary

Effect of High-flow nasal cannula oxygen on end-expiratory lung volumes determined by electrical impedance tomography

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.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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 Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• High-flow nasal cannula oxygen

Locations
Country Name City State
France CHU Clermont-Ferrand Clermont-Ferrand

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary End-expiratory lung volume (EELV) determined by electrical impedance tomography before NIV non invasive ventilation at day 1 No
Primary End-expiratory lung volume (EELV) determined by electrical impedance tomography during NIV non invasive ventilation at day 1 No
Primary End-expiratory lung volume (EELV) determined by electrical impedance tomography after NIV non invasive ventilation at day 1 No
Secondary Anterior, medio-anterior, medio-posterior and posterior EELV at each time at day 1 No
Secondary Diaphragmatic excursion and thickness determined by ultrasound at day 1 No
Secondary Ventilatory frequency at day 1 No
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