AzTrials
AzTrials

Liver Transplant FailureGLYGALTNCT05866796

Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

An observational study of Liver Transplant Failure and Prognostic Biomarkers, run by University Hospital, Ghent at 1 site in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
GlycoTransplantTest
How many people
600 participants
Where
1 siteBelgium
Study dates
26 Apr 2023to 31 Mar 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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

Who may be able to join

  • Signed and dated patient informed consent document
  • Age ≥ 18 years
  • Ability to comply with protocol-specified evaluations and scheduled visits
  • Diagnosis of end-stage liver disease, primary hepatic malignancy 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

Who cannot join

  • Transplantation of one or more organs not including the liver

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Xavier Verhelst, MD, PhD contact

0032 9 332 23 71

xavier.verhelst@uzgent.be

Belgium1 site, 1 recruiting
  • Xavier Verhelst

    Ghent, Flanders, 9000

    Xavier Verhelst, MD, PhD, +3293322371, xavier.verhelst@uzgent.be

    Lorenz Grossar, MD, +32494088789, lorenz.grossar@uzgent.be

    Recruiting

Other trials in Belgium

About this study

Official title: Validation of Serum GLYcomics to Predict Graft Loss and Mortality After Liver Transplantation

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).

Read more

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.

Being tested
GlycoTransplantTest
Keywords
Glycomics, Liver transplantation, Graft survival

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GlycoTransplantTestDiagnostic test

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

Study groups in NCT05866796
Study groupRoleWhat they receive
No graft lossPatients receiving liver transplantation that do NOT experience graft loss within 3-months or 12-months after liver transplantation.
Receives: Diagnostic Test: GlycoTransplantTest
Graft lossPatients 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.
Receives: Diagnostic Test: GlycoTransplantTest

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Graft loss

    Death or need for retransplantation

    Measured: 3 months after liver transplantation

  2. Mortality

    All-cause mortality

    Measured: 3 months after liver transplantation

Secondary outcomes (2)
  1. Graft loss

    Death or need for retransplantation

    Measured: 12 months after liver transplantation

  2. Mortality

    All-cause mortality

    Measured: 12 months after liver transplantation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 May 2023
  2. Study start26 Apr 2023
  3. Primary completion31 Mar 2028 (estimated)
  4. Study completion31 Mar 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05866796
Sponsor's protocol ID
ONZ-2023-0061
Acronym
GLYGALT
Status last verified
Sep 2026
First submitted
10 May 2023
Last updated
21 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Transplant Failure and Prognostic Biomarkers, run by University Hospital, Ghent at 1 site in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Xavier Verhelst, MD, PhD (0032 9 332 23 71, xavier.verhelst@uzgent.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Graft loss (time frame: 3 months after liver transplantation). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Sep 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in