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Usefulness of Alpha-GST in Liver Transplantation (GST-LT)

B

Beaujon Hospital

Status

Unknown

Conditions

Evidence of Liver Transplantation

Study type

Observational

Funder types

Other

Identifiers

NCT02451046
2015-A00839-40

Details and patient eligibility

About

The primary objective of this study was to evaluate the ability of plasma alpha-GST measurements in liver donor (at the time of organ removal) to predict primary dysfunction in liver recipient. The secondary objective was to study the relationship between alpha-GST levels in the plasma of the liver transplant recipient and early graft function recovery.

Full description

Graft primary dysfunction (PDF) after liver transplantation is enhanced by the increasing use of extended-criteria allografts. This complication is burdened with high mortality and morbidity rates among liver transplant recipients. Alpha-GST is a short-life hepatocyte enzyme that may be an interesting biomarker for liver injury. A recently developped ELISA technique may allow fast and easy measurement of alpha-GST plasma concentration (Fastpack IP α-GST Immunoassay, Qualigen Inc., Carlsbad, CA). This study aims to evaluate the ability of plasma alpha-GST measurements in liver donor to predict PDF in liver recipient. Methods: Observational study conducted in one center (Beaujon hospital, APHP, Clichy, France). Measurements of plasma levels of alpha-GST using Fastpack IP α-GST Immunoassay (Qualigen Inc., Carlsbad, CA) at the time of organ removal in liver donor and daily from day 0 to day 7 after liver transplantation in recipients.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age > 18 years
  • undergoing liver transplantation at Beaujon hospital (APHP, Clichy, France )

Exclusion criteria

  • age >70 years and <18 years

Trial contacts and locations

1

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Central trial contact

Emmanuel Weiss, MD; Catherine Paugam-Burtz, MD-PhD

Data sourced from clinicaltrials.gov

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