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NCT02138903 Clinical Trial

A Cardiac Ultrasound Evaluation of Two Types of Weaning Trials of Mechanical Ventilation for a First Weaning Trial

Critical Care Clinical Trial

— CARWEAN  

Official title:
A Cardiac Ultrasound Evaluation of Two Types of Weaning Trials of Mechanical Ventilation for a First Weaning Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02138903
Other study ID # CHU-189
Secondary ID 2013-000960-26
Status Completed
Phase N/A
First received April 11, 2014
Last updated November 28, 2014
Start date January 2014
Est. completion date November 2014

Study information
Verified date November 2014
Source University Hospital, Clermont-Ferrand
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

Comparing the hemodynamic and cardiac effects of two types of weaning trials of mechanical ventilation in ICU patients of two French ICU.

Description:

Prospective clinical study in ICU with ventilated patients eligible to weaning trials of mechanical ventilation (ZEEP and tubing-spontaneous ventilation) comparing hemodynamic and cardiac effects evaluated by trans-thoracic echocardiography.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients ventilated requiring first weaning trial of mechanical ventilation

- Stable respiratory and hemodynamic conditions

- Consent of patients or family

- Arterial line

- Ventilated patients

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• trans thoracic echocardiography

Locations
Country Name City State
France CHU de 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 left ventricular filling pressure Echo-cardiographic evaluation is realized at the end of the weaning trial (1 hour) or less if failed after 1 hour No
Secondary Comparison of other echocardiographic parameters of left ventricular filling pressures Comparison of other echocardiographic parameters of left ventricular filling pressures (E, Ea, deceleration time) at the end of weaning trial after 1 hour No
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