Screening At-risk Populations for Hepatic Fibrosis With Non-invasive Markers

Recruiting N/A Interventional Study
Liver Diseases, Alcoholic Fibrosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
30 – 75
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
6,500 (estimated)
Sponsor
Maja Thiele · Other
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About This Trial

Prospective screening study at Odense University Hospital to assess the effect of transient elastography and other serum and imaging markers of liver fibrosis to detect advanced fibrosis (Kleiner Fibrosis score F3-F4) in patients at risk of non-alcoholic fatty liver disease, alcoholic fatty liver disease, with a control group of participants recruited from the general population.

Trial Locations
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Eligibility Criteria
INCLUSION CRITERIA Patients are eligible for screening if the following inclusion criteria are fulfilled: * Age 30-75 years (except the general population, which should be aged 40-75) * Informed consent to study investigations * Ability to read and write Danish AND (only at-risk patients) * Prior …
Contacts

Maja Thiele, MD, PhD, Professor

+4524998068

maja.thiele@rsyd.dk

CONTACT