No registrations found.
ID
Source
Brief title
Health condition
major surgery with large fluid shifts, Hemodynamic Monitoring, fluid responsiveness, contractile function of both left and right ventricles
Sponsors and support
Laarbeeklaan 101
1090 Jette
Belgium
Laarbeeklaan 101
1090 Jette
Belgium
Intervention
Outcome measures
Primary outcome
Diagnosis of fluid responsiveness and ventricular failure at the hereunder described timepoints.
Secondary outcome
N/A
Background summary
In a comparative prospective study a disposable TEE will be used to compare diagnosis of fluid responsiveness and ventricular failure in high risk surgical patients. The comparative monitoring will be a non-invasive haemodynamic monitor, providing beat-to-beat cardiac output and blood pressure variability (Nexfin).
Study objective
This study aims to investigate the value and feasibility of a disposable TEE to monitor both fluid responsiveness and global contractile function of both left and right ventricles in high risk surgical patients, including both intraoperative management and postoperative follow up in a high dependency unit of a university hospital, against the information obtained from a non-invasive hemodynamic monitoring tool.
Study design
After induction of anesthesia, at each period of hemodynamic instability, before extubation, and in the postoperative phase on arrival in the high-dependency unit and every 4 hrs thereafter. Whenever hemodynamic instability occurs, an evaluation in addition will be performed.
Intervention
Insertion of an echoprobe in the oesophagus via nose. The tool is used solely for hemodynamic monitoring. The final diagnosis is performed by the attending anesthetist.
Veerle Mossevelde, van
Brussels 1090
The Netherlands
+32 (0)2 4763134
veerle.vanmossevelde@uzbrussel.be
Veerle Mossevelde, van
Brussels 1090
The Netherlands
+32 (0)2 4763134
veerle.vanmossevelde@uzbrussel.be
Inclusion criteria
All patients (aged between 18 and 75 y) are scheduled for high-risk abdominal, gynecological, vascular or orthopedic surgery.
Exclusion criteria
Excluded are those patients undergoing upper gastro-intestinal surgery with an impossibility to perform a TEE investigation. Also not enrolled are patients suffering from coagulopathy, or inability to insert a transesophageal probe for whatever medical reason.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL3176 |
NTR-old | NTR3320 |
Other | MEC UZ Brussel : 2011/214 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |