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RecruitingNCT06307964HepMAHUpdated Feb 10, 2026

Intra-Hepatic Microbiota in Alcoholic Hepatitis

An observational study in Cirrhosis, Alcoholic Liver Disease and Alcoholic Hepatitis, sponsored by Hospices Civils de Lyon. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-10.

Sponsored by Hospices Civils de Lyon · Observational

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Alcoholic hepatitis (AH) is a serious complication of alcoholic liver disease (ALD). The histological presentation of AH is characterized by neutrophilic lobular inflammation, macrovesicular steatosis, hepatocyte ballooning and necrosis and the presence of Mallory bodies. In cases of severe HA, defined by a modified Maddrey score of 32 or above, mortality at 1 month is estimated at between 10 and 50%. The only treatment to reduce early mortality is corticosteroid therapy. However, only 60% of patients respond to corticosteroids, and no benefit has been demonstrated on late mortality. Identifying new therapeutic targets is therefore a major challenge in this disease.

Numerous pre-clinical studies and human data suggest the involvement of the intestinal microbiota in the pathogenesis of AH. Translocation of viable bacteria and microbial products from the digestive tract to the liver contributes to local and systemic inflammation, hepatocyte death and fibrogenesis. However, the intrahepatic microbial environment has never been characterized in HA.

The study hypothesis is that the intrahepatic microbiota is modulated by bacterial translocation and is associated with clinical outcomes.

The aim of this study is to determine the composition of the intrahepatic (obtained from transjugular liver biopsy), blood and fecal microbiota in patients with suspected severe AH from a monocentric prospective cohort in the Hepatology Department at Croix-Rousse Hospital (Lyon). Fifty consecutive patients with clinical suspicion of AH and indication for transjugular liver biopsy will be included. About thirty-five patients are expected in the confirmed AH group, and 15 in the group "alcoholic liver disease with no AH", based on data from the literature. The composition of the various microbiota will be determined by sequencing the 16S rRNA gene, and the results will be correlated with clinical data (corticosteroid sensitivity, overall survival, transplant-free survival, MELD score in particular) and histological data.

This exploratory study will enable to analyze the intra-hepatic microbiota, and to study its link with intra-hepatic inflammation and the clinical course of patients with AH. The data generated by HepMAH will thus help identify potential new therapeutic targets linked to the gut microbiota, and provide a scientific basis for the development of therapeutic interventions targeting the microbiota in HA.

02

Conditions studied

  • Cirrhosis
  • Alcoholic Liver Disease
  • Alcoholic Hepatitis

Keywords

  • alcoholic hepatis
  • bacterial translocation
  • microbiota
  • 16S rRNA
  • intra-hepatic microbiota
  • cirrhosis
  • alcoholic liver disease
03

In context

Fibrosis

3,255 studies on the registry are indexed under Fibrosis; 465 are open to participants now.

This study's planned enrollment of 50 is below the median of 110 across 973 observational studies indexed under Fibrosis.

Browse Fibrosis studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,826 studies on the registry; 439 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

A prospective observational multicentric cohort will be conducted at Croix Rousse Hospital (Lyon, France), in the Hepatology and Intensive Care Units.

Fifty consecutive patients hospitalized in either of these units for clinical suspicion of alcoholic hepatitis and indication for transjugular liver biopsy will be included.

Inclusion criteria

  • Patients suffering from alcoholic liver disease and clinical suspicion of alcoholic hepatitis (subacute jaundice, heavy alcohol consumption active or weaned for ≤ 3 months, modified Maddrey score ≥32) and indication for diagnostic transjugular liver biopsy;
  • Non-objection obtained from the patient or trusted person in case of impaired judgment or consciousness before performing liver biopsy;
  • Aged ≥ 18 years at the time of study entry;

Exclusion criteria

Exclusion Criteria:

  • Patients who were treated with antibiotics or probiotics between the 15th day and 72 hours prior to liver biopsy, with the exception of antibiotics used for the prophylaxis of ascites infection or hepatic encephalopathy
  • Contraindication to transjugular liver biopsy (hepatocellular carcinoma on predicted puncture site)
  • Pregnant, parturient or breast-feeding women
  • Persons deprived of their liberty by judicial or administrative decision
  • Adults under legal protection (guardianship, curators)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Alcoholic hepatitis

    Patients with histologically proven AH (after transjugular liver biopsy procedure and histological assessment).

    Procedure: Biological sampling

  • No alcoholic hepatitis

    Patients with initially suspected AH (excessive alcohol consumption and modified Maddrey score \> 32) but no AH at the histological evaluation of liver biopsy. It corresponds to patients with decompensated alcoholic liver disease but no AH.

    Procedure: Biological sampling

Interventions

  • ProcedureBiological sampling

    * A fragment of the diagnostic transjugular liver biopsy (D0) * Plasma samples at D0, and at 1 and 6 months after liver biopsy if possible * Fecal samples at D0, and at 1 and 6 months after liver biopsy if possible

06

What researchers measure

Primary outcomes

  1. Microbiota composition

    Intrahepatic, blood and fecal microbiota composition will be assessed by 16S rRNA sequencing (MiSeq Illumina). Microbiota analysis will be performed on the fragment of transjugular liver biopsy collected for the purpose of the study, and on plasma and fecal samples after bacterial DNA extraction. Bioinformatics analysis will be carried out using Qiime2, LeFSE (Conda) and the Maaslin2 package (v3.16; R software). Microbiota profiles determined at the genus taxonomic level will be compared between the two groups (proven AH and no AH).

    Time frame: At Day 0, 1 month and 6 months

07

Study locations

1 of 1 sites recruiting
  • Hospices Civils de Lyon, Croix Rousse Hospital
    Lyon, France
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06307964
Lead sponsor
Hospices Civils de Lyon
Responsible party
Sponsor
First posted
Mar 13, 2024
Start date
Jul 23, 2024
Primary completion
Jan 23, 2028 (estimated)
Completion
Jul 23, 2028 (estimated)
Last update
Feb 10, 2026

Study contacts

François VILLERET, M.D., Ph.D.
Contact
francois.villeret@chu-lyon.fr
+33426109382
François VILLERET, M.D., Ph.D.
study chair · Hospices Civils de Lyon, Croix Rousse Hospital, Hepatology department

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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