Clinical Trials Directory

Trials / Completed

CompletedNCT02678559

Preload Dependency Evaluation With Stroke Volume Variation During Alveolar Recruitment Manoeuvres

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
24 (actual)
Sponsor
University Hospital, Clermont-Ferrand · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The principal aim is to assess impact of alveolar recruitment manoeuvres (ARM) on stroke volume variation, evaluated by trans-oesophageal echocardiography (TEE). These variations will be measured on preload dependency or preload independency status. The principal purpose is to determine if variations of stroke volume during standardized ARM can predict the preload dependency status.

Detailed description

Population studied: anesthetized patients for cardiac surgery of coronary bypass. Secondary endpoints : - comparison between TEE and mini-invasive monitoring systems in accuracy of measurement of stroke volume variation during ARM. These mini-invasive systems are : Clearsight system (Edwards Lifescience) and Flotrac system (Edwards Lifescience) \- Difference between pre and post-cardiopulmonary bypass status on principal purpose evaluation

Conditions

Interventions

TypeNameDescription
OTHERtee measurement
OTHERflotrac measurement
OTHERclearsight measurement

Timeline

Start date
2016-02-01
Primary completion
2016-12-01
Completion
2016-12-01
First posted
2016-02-10
Last updated
2017-04-20

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02678559. Inclusion in this directory is not an endorsement.