About this trial
The rational to conduct the LOVE study builds on the lack of available data on outcomes in steatotic liver disease in well characterized patients over a time frame of several years. At current limited data on liver-specific and overall outcome in patients with MASLD, MetALD and ALD are available. Liver histology is the only accepted surrogate to reasonably likely predict outcomes in patients with non-cirrhotic liver disease and is currently used in regulatory trials. To overcome the limitations of liver biopsy and use validated non-invasive tests (NITs) to predict outcomes, the LOVE study will be conducted based on existing cohort studies in well pheno- and genotyped patients and will inform on the relevant outcomes based on baseline and ongoing biomarker assessment. The overarching goal is to qualify a NIT for patient identification and preventive measures in the regulatory context.
Eligibility criteria
Qualifiers
Previous Informed consent for cohort studies
> 18 years of age
Diagnosis of SLD (MASLD, MetALD, ALD)
Disqualifiers
No consent for previous cohort studies
< 18 years of age
No Diagnosis of SLD (MASLD, MetALD, ALD)
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Universität des Saarlandes
Lead sponsor
Universitatsmedizin Mainz - 1. Medizinische Klinik
Collaborator
Newcastle University
Collaborator
Barcelona Institute for Global Health
Collaborator
Odense University Hospital
Collaborator
Hospital Clinic of Barcelona
Collaborator
Assistance Publique - Hôpitaux de Paris
Collaborator
University of Turin, Italy
Collaborator