Lung Aeration During WEANing From Mechanical Ventilation Determined by Electrical Impedance Tomography and Lung Ultrasound

Critical Care Clinical Trial

— IWEAN  

Official title:

Lung Aeration During WEANing From Mechanical Ventilation Determined by Electrical Impedance Tomography and Lung Ultrasound

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02361021
• Other study ID #: CHU-0222
• Status: Recruiting
• Phase: N/A
• First received: February 2, 2015
• Last updated: July 23, 2015
• Start date: July 2015
• Est. completion date: August 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: Commission nationale de l'informatique et des libertés
• Study type: Observational

Clinical Trial Summary

Evaluation of lung aeration during weaning from mechanical ventilation determined by electrical impedance tomography and lung ultrasound

Description:

Prospective clinical study in ICU with patients during weaning from mechanical ventilation comparing lung aeration determined by electrical impedance tomography and lung ultrasound.

Duration of weaning test is 60 minutes.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: August 2015
• Est. primary completion date: August 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult ICU patients during weaning test from mechanical ventilation

• 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

• Critical Care
• Electrical Impedance Tomography
• End Expiratory Lung Volume
• Lung Ultrasound Score
• Weaning From Mechanical Ventilation

Intervention

Other:
• - Weaning from mechanical 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)	End-expiratory lung volume (EELV) determined by electrical impedance tomography at baseline (start of the weaning test)	at baseline	No
Primary	End-expiratory lung volume (EELV)	- End-expiratory lung volume (EELV) determined by electrical impedance tomography at Hour 1 (end of the weaning test).	at hour 1	No
Secondary	Anterior, medio-anterior, medio-posterior and posterior EELV		at baseline (start of the weaning test)	No
Secondary	Lung ultrasound score		at baseline (start of the weaning test)	No
Secondary	Anterior, medio-anterior, medio-posterior and posterior EELV		at Hour 1 (end of the weaning test)..	No
Secondary	Lung ultrasound score		at Hour 1 (end of the weaning test)..	No