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Clinical Trials in Germany / NCT05810480
Recruiting Observational

PredIcting sterOid depeNdEnt livEr injuRy With Polyreactive Immunoglobulin G

NCT05810480 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2023-06-06
Last updated
2026-07-15

Condition(s) studied

Autoimmune HepatitisAutoimmune Liver Disease

Investigational drug(s) / intervention(s)

polyreactive immunoglobulin G

polyreactive immunoglobulin G: Polyreactive immunoglobulin G will be tested centralized in Hannover as published (Taubert, Engel et al., Hepatology, 2022). The current standard diagnostic autoantibodies (e.g. ANA, anti-SMA, anti-LKM, anti-LC1, anti-SLA/L) will be tested centrally in Hannover according to current guidelines.

Study summary

The investigators identified polyreactive immunoglobulin G (pIgG) in adults (published in Hepatology: https://doi.org/10.1002/hep.32134) and children (in preparation). Quantification of these pIgG using a "home-made" ELISA facilitates the diagnosis of autoimmune hepatitis (AIH) as compared to non-AIH liver diseases and healthy controls. Positivity for pIgG was independent from ANA/SMA positivity and equally diagnostic for AIH even when conventional autoantibodies (ANA/SMA/SLA/LKM) were negative.

Additionally, the frequency of pIgG was lower than conventional autoantibodies (ANA, SMA) in vaccinia/drug associated severe liver injury in a retrospective multicenter study after Covid-19 vaccination (https://doi.org/10.1016/j.jhepr.2022.100605).

Aims of the study The study aims to evaluate the diagnostic capacity of pIgG to predict AIH in comparison to other liver diseases prospectively. To avoid diagnostic inaccuracy between AIH with long-term need for an immunosuppression and drug induced liver injury with autoimmune features, which can be indistinguishable from AIH at baseline and which has a very low relapse rate after a short steroid course, a follow-up after six months is obligatory for inclusion.

Therefore, the investigators will collect one serum sample from every patient (without immunosuppressive treatment) that presents to the respective hospital for evaluation of liver disease by liver biopsy within one year after initiation of the study and that provided written informed consent. Follow-up for evaluation of steroid dependency at six months after diagnosis is obligatory.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Diagnostic liver biopsy for the work-up of any liver disease * Informed consent * Definition of any liver disease according to current societal guidelines Exclusion Criteria: * Ongoing immunosuppression at the liver biopsy or prior to the liver biopsy * Liver biopsies for the grading or staging of an already known liver disease (e.g. non-alcoholic fatty liver disease (NAFLD), Hepatitis B/D Virus Infections (HBV/HDV Infection), …) * known liver disease * missing informed consent * patients or caregivers who can not provide informed consent

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
RWTH Aachen Aachen Germany Not Yet Recruiting
University Medical Center Hamburg-Eppendorf Hamburg Germany Not Yet Recruiting
Hannover Medical School Hanover Germany Recruiting
University Medical Center Heidelberg Heidelberg Germany Not Yet Recruiting
University Hospital Schleswig-Holstein, Location Lübeck Lübeck Germany Not Yet Recruiting
Rostock University Medical Centre Rostock Germany Not Yet Recruiting

More Hannover Medical School trials in Germany

Other trials for the same condition

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 NCT05810480 on ClinicalTrials.gov ↗ ← All trials in Germany