Clinical Trials in Italy / NCT06749990
Recruiting
Observational
Risk and Protective Factors for Relapse to Alcohol Use in Patients With Liver Disease Undergoing Liver Transplantation
NCT06749990 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Alcohol Related Liver DiseaseOrthotopic Liver Transplantation
Study summary
This is an observational, monocentric study, consisting of both a retrospective and a prospective component. The aim of the study is to identify risk and protective factors for alcohol relapse in patients with alcohol-related liver disease (ARLD) who have undergone orthotopic liver transplantation (OLT).
Eligibility
Inclusion Criteria:
* Patients who have signed the informed consent
* Candidates for liver transplantation due to liver disease with alcohol-related etiology (either mono- or multifactorial)
* For the retrospective part: patients who underwent OLT for ARLD during the time frame 2017-2022
Exclusion Criteria:
* Major psychopathologies and active psychoses
Primary outcome measure(s)
- alcohol relapse rate — 7 years
To describe the population undergoing liver transplantation with a diagnosis of ARLD and exotoxicity-related components in terms of alcohol relapse rate - alcohol recurrence rate — 7 years
To describe the population undergoing liver transplantation with a diagnosis of ARLD and exotoxicity-related components in terms of alcohol recurrence rate - Clinical data to assess the risk of alcohol relapse — 7 years
Collection of clinical data on liver disease through routine visits to assess the risk of alcohol relapse at 12 months post-OLT - psychiatric evaluation to assess the risk of alcohol relapse — 7 years
Administration of a clinimetric assessment composed of psychometric, self-assessment tests, already validated and widely used in the literature
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06749990 on ClinicalTrials.gov ↗ ← All trials in Italy