Clinical Trials Directory

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UnknownNCT02451046

Usefulness of Alpha-GST in Liver Transplantation

Predictive Ability of Alpha-GST to Detect Graft Primary Dysfunction After Liver Transplantation

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Beaujon Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed 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.

Conditions

Timeline

Start date
2014-03-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2015-05-21
Last updated
2015-05-21

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02451046. Inclusion in this directory is not an endorsement.