CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 297 enrolled
Drug / intervention
Amoxicillin +2 moredrug
Likely dose
Amoxicillin 375 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02281929
NCT02281929Phase 3Completed

Evaluation of the Efficacy of an Antibiotic Combined With Standard Treatment in Severe Alcoholic Hepatitis

University Hospital, Lille·interventional·Posted Nov 4, 2014·Updated Dec 22, 2025

In Brief

A Phase 3 clinical trial evaluating Amoxicillin, Placebo, and 1 other intervention for Alcoholic Hepatitis and Alcoholic Liver Disease. Completed, enrolled 297 participants across 20 sites.

Detailed Summary

Treatment of reference of severe alcoholic hepatitis is based on corticosteroids, given for 28 days. However, about 25-35% of patients do not take benefit from this treatment and die within the 6 months following the diagnosis. Numerous trials have evaluated the impact of several strategies in association with corticosteroids. None of them has shown an improvement in survival (primary endpoint) as compared to corticosteroids alone. The project is based on an approach never tested in a randomized controlled trial in severe alcoholic hepatitis, targeting the group of patients at high risk of death (25-35% at 2 months). This approach is based on animal and human studies.Antibiotics are effective in animal models and in other circumstances characterized by liver failure such as gastrointestinal bleeding related to portal hypertension. The interest of studying this population is emphasized by the frequency of infections in these critically ill patients. Antibiotics will be administered before the development of any infection, as it is likely that these patients present with mesenteric bacterial adenitis without systemic signs of infection. Primary endpoint will be 2-month survival as most deaths occur within 60 days and treatment is given for 30 days.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedNov 4, 2014
Enrollment StartJun 13, 2015
Primary CompletionNov 19, 2019
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 11.7 years ago

Interventions

Amoxicillindrug

Amoxicillin+clavulanic acid at a daily dose of 3 gram / 375 mg in three daily doses of 1g/125mg, during 30 days

Placebodrug

Placebo in three daily doses during 30 days

Prednisolonedrug

Prednisolone at 40 mg/j in a single daily dose in the morning, during 30 days