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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02150018
Other study ID # CHU-0193
Secondary ID
Status Recruiting
Phase N/A
First received May 26, 2014
Last updated July 30, 2015
Start date June 2014
Est. completion date December 2015

Study information

Verified date July 2015
Source University Hospital, Clermont-Ferrand
Contact Patrick LACARIN
Phone 04 73 75 11 95
Email placarin@chu-clermontferrand.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

Effect of Non Invasive Ventilation on end-expiratory lung volumes determined by electrical impedance tomography


Description:

Prospective clinical study in ICU with patients requiring non invasive ventilation (NIV) comparing lung volumes determined by electrical impedance tomography before, during and after NIV.

Duration of NIV is 30 minutes.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult ICU patients requiring non invasive ventilation

- Consent of patients or family

- Arterial line

Exclusion Criteria:

- Tracheotomized patients

- Dressings in the thoracic area

Study Design

Time Perspective: Cross-Sectional


Intervention

Other:
non invasive ventilation


Locations

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

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand University Hospital, Estaing

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, during and after NIV at day 1 No
Secondary Anterior, medio-anterior, medio-posterior and posterior EELV at day 1 No
Secondary Ventilatory frequency at day 1 No
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