Addictolive: Addiction Intervention in Liver Transplantation Candidates

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Recruiting
CT.gov ID
NCT05322226
Collaborator
(none)
130
1
1
33.1
3.9

Study Details

Study Description

Brief Summary

Addiction care is "a la carte treatment", adapted to the motivation and time constrains of users. Thus, various types of psychotherapeutic follow-up can be considered, different addictolytic medications or opioid maintenance therapies can be offered during treatment and hospitalization must be adaptable. In liver transplantation (LT), sustained alcohol relapse is a critical issue because it increases medium and long-term morbidity and mortality. In recent years, the issue of severe acute alcoholic hepatitis as an indication for LT has necessitated increased focus on appropriate alcohol monitoring around liver transplantation. Previously, alcohol consumption in pre- and post-LT period was mainly self-reported. More recently, the biological markers of excessive alcohol consumption have been validated in liver disease and can play a role in liver transplant recipients follow-up.

The investigator hypothesize that standardized targeted addiction monitoring of LT patients decreases the rates of sustained alcohol relapse one year post liver transplantation.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Addiction follow-up before and after liver transplantation
N/A

Detailed Description

The main objective of this study is to identify the impact of a targeted addiction monitoring of pre- and post-LT patients on rates of sustained alcohol relapse, one year after LT at the Liver Transplant Unit of the University Hospital of Montpellier. The secondary objectives are: (i) to precisely detail all the addiction treatments (medications, psychotherapy types and specific hospitalization) implemented during this follow-up, (ii) to assess the impact of targeted addiction treatment on the tobacco use and other psychoactive substances (PS) consumption rates , (iii) to quantify LT patients' acceptability of referral to addiction-related treatment and care, (iv) to assess the relevance of biological markers of excessive alcohol consumption during pre- and post-LT period.

The investigator will conduct an A'Hern Single-stage Phase II monocentric interventional trial.

All patients undergoing assessment for LT in Montpellier's Liver Transplant Unit will be consecutively included during their first systematic consultation with the addiction specialist. During this interview, the risk of alcohol relapse will be assessed and targeted addiction follow-up will be planned. Starting from the registration on the national waiting list, biological markers of excessive alcohol consumption will be performed every three months and the patient will be referred to the addiction specialist if the results are positive. After LT these evaluations will continue every three months for one year and patients will be referred for addiction treatment as needed. All participants will have a final interview with an addiction specialist one year post LT.

Using the single-stage A'Hern design, a sample size of 65 LT patients is required to distinguish between a maximum futility proportion of 26% of sustained relapses and a minimum efficacy proportion of 13%, with a one-sided significance level of 0,047 and a power of 82,4%. Based on these criteria, the number of patients with sustained relapse must be at least 10 for the proposed treatment to be deemed effective.

Each patient's socio-demographic, medical, hepatological and addiction data will be collected at baseline. All data concerning each patient's targeted addiction follow-ups, biological markers, rates of sustained alcohol relapse, tobacco and PS consumption rates will be noted during the first year after LT.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
130 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluation of an Addiction Intervention in Candidates for Liver Transplantation
Actual Study Start Date :
Jul 27, 2022
Anticipated Primary Completion Date :
Jan 1, 2025
Anticipated Study Completion Date :
May 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Adults undergoing pre- liver transplant assessment

All patients included in the study will have blood and urinary test from their registration on the transplant list and during their classic follow-up with their hepatologist for 12 months to quantify the biological markers of alcoholism (every 3 months). Additional tubes and urine will be collected in order to measure these markers (urinary ethylglucuronide and blood phosphatidylethanol).

Behavioral: Addiction follow-up before and after liver transplantation
Addiction consult and follow-up

Outcome Measures

Primary Outcome Measures

  1. Rate of liver transplant patients with sustained alcohol relapse one year after liver transplant [1 year]

    The rate is defined by at least one positive alcohol marker and a daily amount of alcohol exceeding 3 (women) or 4 (men) drinks per day with the notion of loss of control recorded during addiction interview

Secondary Outcome Measures

  1. Description of addictological means implemented during follow-up. [1 year]

    Addiction physician will choose medications, psychotherapeutic interventions, and hospitalization when appropriate. Rate of patients in pre-transplantation evaluated at low risk and with severe relapse at 1 year post liver transplant.

  2. Addiction consult [1 year]

    Rate of patient complying with their appointment

  3. Addiction consult following biology results [1 year]

    Proportion of follow-up addiction consultations having been guided, according to the opinion of the clinician, by the results of the biological markers (and not only by the self-declaration of consumption).

  4. Caracterization of contraindicated patients [1 year]

    Rates and characteristics of patients with temporary and/or permanent addiction contraindication

  5. Rate of transplanted patients with tobacco and other psycoactive substance consumption during the first year after liver transplant [Every 3 months during 1 year]

    Smoking cessation is defined declaratively and using an expired CO test (< 6.5 ppm). Psychoactive substance consumption is declarative.

  6. Description of urinary marker of alcohol consumption. [Every 3 months during 1 year]

    Urinary Ethylglucuronid (sensitiviy of 62-89% and specificity of 93-99% for alcohol absoption within 30 to 80 hours before urinary test.)

  7. Description of blood marker of alcohol consumption. [Every 3 months during 1 year]

    Blood phosphatidylethanol (sensitivity of 90-99% and specificity of 100% for alcohol absorption within 2 to 6 weeks before blood test.)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • all adults undergoing pre-transplant assessment in the Liver Transplantation Unit of University Hospital of Montpellier, providing oral informed consent.
Exclusion Criteria:
  • Patients under protection of justice or unable to receive a clear information.

  • Exclusion period determined by previous study

  • Pregnent women or breastfeeding

  • Patient under guardianship or curatorship

  • Not affiliated to french social security

Removal of subjects from study criteria:

not registered on the liver transplant waiting-list or not transplanted during the study period.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of hepato-gastroenterology and liver transplantation Montpellier Occitanie France 34090

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

  • Principal Investigator: Helene Donnadieu, MH PD, Montpellier University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT05322226
Other Study ID Numbers:
  • RECHMPL21_0516_UF7932
First Posted:
Apr 11, 2022
Last Update Posted:
Aug 2, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Montpellier
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2022