Endotracheal Cardiac Output Monitor (ECOM) for Patients Undergoing Liver Transplantation

Mayo Clinic

Status: Terminated

Conditions: Liver Transplantation

Treatments: Device: ECOM ETT

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT01299441

10-007600

Details and patient eligibility

About

The purpose of this study is to determine whether the endotracheal cardiac output monitor (ECOM) is accurate and predictive in liver failure patients with hyperdynamic circulatory changes.

Enrollment: 40 patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients undergoing liver transplantation surgery

Exclusion criteria

• Patients who are anticipated to remain intubated postoperatively for greater than 24 hours.

Trial design

40 participants in 1 patient group

OLT patients intubated with ECOM ETT

Description:

Patients undergoing liver transplantation and intubated with ECOM endotracheal tube (ETT).

Treatment:

Device: ECOM ETT