ClinicalTrials.gg
RecruitingNCT05866796GLYGALTUpdated Sep 21, 2026

Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

An observational study in Liver Transplant Failure and Prognostic Biomarkers, sponsored by University Hospital, Ghent. Recruiting at 1 site in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by University Hospital, Ghent · Observational

From the registry’s dates

  • Started Apr 2023; still recruiting 3 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
600
Ages
18 Years and older
Sex
All
01

Study summary

The first 12 months after liver transplantation (LT) are decisive in posttransplant outcome, as almost half of deaths and two thirds of graft loss requiring retransplant occur in the first year after LT. Since delaying retransplantation in those patients that experience an unfavorable posttransplant course directly impacts their outcome, timely decision making is of paramount importance in these individuals. However, balancing the need and right timing for retransplantation in individual patients with a complicated posttransplant course is currently a difficult challenge that relies on imperfect clinical variables and biomarkers, as well as the experienced judgment of the transplant team.

Building on the findings of a pilot study in liver transplant recipients (n = 131) led by the Ghent University Hospital, we want to validate the prognostic performance of the GlycoTransplantTest on a multicentric scale. In this pilot study, a single glycomic signature at day 7 after LT allowed accurate prediction of graft loss at 3 months after LT. The serum glycome of those patients experiencing graft loss was characterized by increased undergalactosylation and an increased presence of fucosylated and triantennary glycans. After statistical modeling, use of an optimized cutoff based on the relative abundance of 13 serum glycans showed a strong association with graft loss at 3 months (odds ratio 70.211; P\<0.001; 95% CI: 10.876-453.23).

Using sequential measurements of serum glycomics in liver transplant recipients, we want to prospectively study and validate the predictive value of the serum glycomic signature for graft survival and overall survival at 3-months (primary end point) and 12-months after liver transplantation (secondary end point).

Determination of the serum glycomic profile is a high-throughput technique that allows to study and quantify the relative abundance of sugar chains (glycans) anchored at specific sites of serum proteins. This technique has shown a very strong prognostic value for graft loss at 3-months after liver transplantation in a pilot study at the Ghent University Hospital.

In this large-scale multicentric prognostic study, we will collect serum samples of liver transplant recipients at fixed time points.

Apart from the serum glycomic profile, we will collect data from the patients electronic record: demographic data (gender, age), data directly relevant to the indication of transplant (eg. imaging for primary liver cancer, lab values for diagnosis of end-stage liver disease), and outcome data (graft survival, overall survival, follow-up time). This list is non-exhaustive.

Using this approach, we will demonstrate the predictive validity of serum glycomics in liver transplant recipients for graft survival and overall survival at 3- and 12-months post-LT. Building on these data, the use of a simple blood test could differentiate patients at risk of graft loss and thus represent a paradigm shift directing these patients to timely treatment adaptations.

02

Conditions studied

  • Liver Transplant Failure
  • Prognostic Biomarkers

Keywords

  • Glycomics
  • Liver transplantation
  • Graft survival
03

In context

Lead sponsor

University Hospital, Ghent is the lead sponsor of 689 studies on the registry; 160 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.

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

04

Who can participate

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

Study population

Adult patients active on the waiting list or undergoing a liver transplantation. All indications for liver transplantations are eligible.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Signed and dated patient document
  • Age ≥ 18 years
  • Ability to comply with protocol-specified evaluations and scheduled visits
  • Diagnosis of end-stage liver disease, primary hepatic meeting the Milan criteria for liver transplantation, or acute hepatic failure
  • Eligible for liver transplantation and/or active on the waiting list for liver transplantation. Individuals eligible and/or active on the waiting list for multiple organ transplantation including the liver (eg. Combined liver and kidney transplantation, or intestinal transplantation) are also eligible for inclusion.
  • Consulted the department of Gastroenterology and Hepatology at Ghent University Hospital

Exclusion criteria

Exclusion Criteria:

- Transplantation of one or more organs not including the liver

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
600 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • No graft loss

    Patients receiving liver transplantation that do NOT experience graft loss within 3-months or 12-months after liver transplantation.

    Diagnostic Test: GlycoTransplantTest

  • Graft loss

    Patients receiving liver transplantation that experience graft loss within 3-months or 12-months after liver transplantation. Graft loss is defined as either death of the liver transplant recipient (all-cause), or need for retransplantation of the liver.

    Diagnostic Test: GlycoTransplantTest

Interventions

  • Diagnostic testGlycoTransplantTest

    Determination of serum glycomics in the early posttransplant stage, using an optimal cutoff based on statistic modeling.

06

What researchers measure

Primary outcomes

  1. Graft loss

    Death or need for retransplantation

    Time frame: 3 months after liver transplantation

  2. Mortality

    All-cause mortality

    Time frame: 3 months after liver transplantation

Secondary outcomes

  1. Graft loss

    Death or need for retransplantation

    Time frame: 12 months after liver transplantation

  2. Mortality

    All-cause mortality

    Time frame: 12 months after liver transplantation

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05866796
Responsible party
Sponsor
First posted
May 19, 2023
Start date
Apr 26, 2023
Primary completion
Mar 31, 2028 (estimated)
Completion
Mar 31, 2028 (estimated)
Last update
Sep 21, 2026

Study contacts

Xavier Verhelst, MD, PhD
Contact
xavier.verhelst@uzgent.be
0032 9 332 23 71
Lorenz Grossar, MD
Contact
lorenz.grossar@uzgent.be
0032 494 088 789

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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