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Conditioning with volatile anesthetics in liver transplantation

Conditioning with volatile anesthetics in liver transplantation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-015890-11-BE
Enrollment
106
Registered
2009-10-14
Start date
2009-11-03
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Liver transplantation MedDRA version: 12.0 Level: LLT Classification code 10024716 Term: Liver transplantation

Interventions

Sponsors

University Hospital Ghent
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime 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

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026