Hemodynamic monitoring with a disposable echoprobe.

Evaluation of Feasibility of TEE Both Intraoperatively and Postoperatively.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON28241

Enrollment

Registered

2012-02-23

Start date

2011-10-15

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

major surgery with large fluid shifts, Hemodynamic Monitoring, fluid responsiveness, contractile function of both left and right ventricles

Interventions

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.

Eligibility

Inclusion criteria

Inclusion criteria: All patients (aged between 18 and 75 y) are scheduled for high-risk abdominal, gynecological, vascular or orthopedic surgery.

Exclusion criteria

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 outcomes

Primary

Measure	Time frame
Diagnosis of fluid responsiveness and ventricular failure at the hereunder described timepoints.	—

Contacts

Public ContactVeerle Mossevelde, van

Laarbeeklaan 101

veerle.vanmossevelde@uzbrussel.be+32 (0)2 4763134

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)