Analyzing liver grafts to predict transplant outcomes
Official title: Tissue Analysis (Histological, Ultrastructural and Molecular) of Liver Grafts as a Predictor of Transplant Outcome.
Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06717542 · Data updated 2026-11-12
This study is testing if certain markers in liver grafts can help predict how well the transplant will work for patients receiving the liver.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna) |
| Status | Recruiting |
| Started | January 17, 2023 |
| Main results expected | July 2027 |
| Study ends | January 2028 |
| Registry record updated | December 5, 2024 |
| Trial ID | NCT06717542 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include liver donors and recipients aged 18 years or older who can provide sufficient tissue for analysis.
✕Probably not a fit
Patients who do not undergo HOPE treatment on their liver grafts may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to identify specific endothelial signatures in liver grafts after undergoing a process called HOPE, which is used prior to transplantation. It involves two patient cohorts: liver donors, who will have a biopsy taken for organ quality assessment, and liver recipients, who will undergo a study-specific biopsy after the transplant. The biopsies will be analyzed using histochemical and immunohistochemical techniques, as well as RT-PCR, to uncover molecular changes that could inform personalized perfusion treatments in the future.
Why it matters
Potential benefit: If successful, this study could lead to improved outcomes for liver transplant patients by enabling personalized treatment strategies.
How similar studies have gone: While the approach of analyzing endothelial signatures in liver grafts is innovative, similar studies have shown promise in understanding transplant outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * For Donors: Availability of enough tissue for histological, immunohistochemical and RT-PCR analysis. * HOPE performed on the liver graft prior to transplantation. * For Recipients: * Availability of enough tissue for histological, immunohistochemical and RT-PCR analysis. * Age greater than/equal to 18 years. Exclusion Criteria: * None
Where it's running
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Italy Recruiting
Study contacts
- Principal investigator: Francesco Vasuri, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Francecso Vasuri, MD
- Email: francesco.vasuri2@unibo.it
- Phone: 0512143761
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.