German SLD-Registry (Deutsches SLD-Register)
NCT04721665
Summary
Characterization of patients with steatotic liver disease (SLD) The German SLD-Registry (Deutsches SLD-Register) a project of the German Liver Foundation (Deutsche Leberstiftung), managed by Leberstiftungs-GmbH Deutschland. The German NAFLD-Registry is financially supported by: Advanz Pharma Specialty Medicine Deutschland GmbH und Gilead Sciences GmbH (Grant to German Livber Foundation) sowie Novo Nordisk Pharma GmbH (directly via Leberstiftungs-GmbH).
Eligibility
Inclusion Criteria: * diagnosed SLD based on the following criteria: 1. typical finding of hepatic steatosis (abdominal ultrasound and/or pathological CAP value (latter is optional) 2. Evaluation of SLD degree by NAFLD Fibrosis score and/or FIB-4-Index and/or transient elastography 3. Evaluation of metabolic syndrome * credible assessment of alcohol consumption * written informed consent Exclusion Criteria: * patients with other hepatologic diseases (chronically viral, metabolic, autoimmune origin * patients receiving hepatotoxic medications over a longer period (e.g. methotrexate, amiodarone, longterm NSAR intake) * malignant disease with a life expectancy \<12 months * participation in clinical interventional/pivotal studies * inability to provide written informed consent
Conditions2
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
NCT04721665