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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04964687
Other study ID # RECHMPL21_0410
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2019
Est. completion date May 30, 2021

Study information

Verified date July 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigator seeks to determine wether integrating an addiction team into a liver transplantation unit improves the prognosis of patients with alcohol-related liver disease requiring liver transplantation. Our hypothesis is that patients managed by an addiction team before and after liver transplantation have less frequent alcohol relapses, thus decreasing the risk of cardiovascular complications, de novo cancer, recurrence of alcohol-related cirrhosis, and consequently increasing their overall survival.


Description:

In this observational, retrospective and multicentre study, investigator seek to determine the effect of integrating an addiction team into liver transplantation unit on prognosis of patients with alcohol-related liver disease requiring liver transplantation. Investigatore plan to compare patients in 2 groups, depending on whether they have received or not specific addiction care before and after transplantation. This study was conducted over a period of 15 years in three French liver transplant units.


Recruitment information / eligibility

Status Completed
Enrollment 616
Est. completion date May 30, 2021
Est. primary completion date May 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - adult patients - who received a liver transplant between January 2000 and December 2015 for alcohol-related liver disease as a primary or secondary indication (hepatocellular carcinoma) - who survived for more than 6 months after their liver transplant. Exclusion criteria: - association of other causes of hepatopathy: viral hepatitis B or C, hereditary hemochromatosis. - death before discharge from hospital after liver transplantation. - patient unwilling to participate to the study

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Liver transplantation
Liver transplantation

Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival of patients transplanted for alcoholic liver disease. Patient time (delay between date of transplantation and date of last news) + state (alive or deceased) Date of last news (at least 5 years for surviving patients)
Secondary Alcohol relapse rate Number of patients with alcohol relapse among all transplanted patients. Date of last news (at least 5 years for surviving)
Secondary Severe alcohol relapse rate Number of patients with severe alcohol relapse among all transplanted patients Date of last news (at least 5 years for surviving)
Secondary Rate of alcohol-related cirrhosis recurrence Number of patients with alcohol-related cirrhosis among all transplanted patients. Date of last news (at least 5 years for surviving)
Secondary Rate of development of cardiovascular risk factors Number of patients developing one or more cardiovascular risk factors (hypertension, dyslipidemia, diabetes, smoking) among all transplanted patients. Date of last news (at least 5 years for surviving)
Secondary Cardiovascular event rate Number of patients with one or more cardiovascular events (coronary syndrome, stroke, arterial disease) among all transplant patients. Date of last news (at least 5 years for surviving)
Secondary De novo cancer-free survival Number of patients developing de novo cancer as a function of time among all transplanted patients Date of last news (at least 5 years for surviving)
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