CClinicalTrials.gg
Status unknownNCT02451046GST-LTUpdated May 21, 2015

Usefulness of Alpha-GST in Liver Transplantation

An observational study in Evidence of Liver Transplantation, sponsored by Beaujon Hospital. Status unknown at 1 site in France. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2015-05-21.

Sponsored by Beaujon Hospital · Observational

The sponsor has not verified this record recently (last verified May 2015), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 70 Years
Sex
All
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Study 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.

Read the 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.

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Conditions studied

  • Evidence of Liver Transplantation

Keywords

  • Liver transplantation
  • Primary dysfunction
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In context

Lead sponsor

Beaujon Hospital is the lead sponsor of 10 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergoing liver transplantation at Beaujon hospital (APHP, Clichy, France)

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • age >70 years and \<18 years
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Target follow-up
7 Days
Patient registry
Yes
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What researchers measure

Primary outcomes

  1. Primary dysfunction (PDF) of liver graft

    To evaluate the ability of plasma alpha-GST measurements in liver donor (at the time of organ removal) to PDF in liver recipient.

    Time frame: First week

Secondary outcomes

  1. Early graft function recovery.

    To study the relationship between alpha-GST levels in the plasma of the liver transplant recipient and early graft function recovery.

    Time frame: First week

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Study locations

1 of 1 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 21, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02451046
Lead sponsor
Beaujon Hospital
Responsible party
Paugam-Burtz (Professor, Beaujon Hospital) — Principal investigator
First posted
May 21, 2015
Start date
Mar 2014
Primary completion
Oct 2015 (estimated)
Completion
Oct 2015 (estimated)
Last update
May 21, 2015

Study contacts

Catherine Paugam-Burtz, MD-PhD
Contact
catherine.paugam@bjn.aphp.fr
140875610 ext. +33
Emmanuel Weiss, MD
Contact
manuweiss@yahoo.fr
603004193 ext. +33
Catherine Paugam-Burtz, MD-PhD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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