Liver transplantation MedDRA version: 12.0 Level: LLT Classification code 10024716 Term: Liver transplantation
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Older than 18 years - Patients undergoing liver transplantation - Total or partial cadaveric liver transplantation Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) no F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: - Patients unable to understand the Flemish or Dutch language - Patients with known or suspected allergy to propofol, soja or egg - Patients with norepinephrine infusion above 15 microg/min - Intensive care patients with severe impairment of renal or pulmonary function (e.g. dialysis, hemofiltration, FiO2>0.5)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Hypothesis Sevoflurane conditioning, applied as pre- and postconditioning in liver transplant recipients, attenuate ischemic-reperfusion injury compared with the i.v. propofol anesthesia. ;Secondary Objective: Complication score (surgical complications);Primary end point(s): Postoperative peak of the transaminase (AST). | — |
Countries
Belgium