Ignite Creation Date:
2025-12-24 @ 2:35 PM
Ignite Modification Date:
2026-02-20 @ 6:34 PM
Study NCT ID:
NCT02678559
Status:
COMPLETED
Last Update Posted:
2017-04-20
First Post:
2016-01-15
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Preload Dependency Evaluation With Stroke Volume Variation During Alveolar Recruitment Manoeuvres
Sponsor:
University Hospital, Clermont-Ferrand
Organization:
Study Overview
Official Title:
Preload Dependency Evaluation With Stroke Volume Variation During Alveolar Recruitment Manoeuvres
Status:
COMPLETED
Status Verified Date:
2017-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PreDeARM
Brief 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
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
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: