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Study identifier: NCT07469319 Synced from ClinicalTrials.gov · August 10, 2026
● Study status: RecruitingBISHOP

Biannual Screening for HCC Offered to Patients With Cirrhosis. Introducing Surveillance for Hepatocellular Carcinoma (HCC) in the Central Denmark Region Using Ultrasound and Alpha-Fetoprotein to Reduce HCC-Related Mortality in Patients With Compensated Non-Viral Cirrhosis

Condition: Hepatocellular Carcinoma (HCC) · Cirrhosis  ·  Sponsor: University of Aarhus

PhaseNA
Planned participants617
Who can joinAll sexes, 40 Years to 79 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where6 locations

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

This study aims to investigate whether repeated 6-monthly screening for hepatocellular carcinoma (HCC) - called "HCC surveillance" - offered to selected patients with chronic liver disease can reduce HCC-related mortality by facilitating earlier detection of HCC. The screening procedure consists of two tests: an ultrasound examination of the liver and a blood sample to measure alpha-fetoprotein. Patients who screen positive on either examination will be offered standard work-up for HCC, typically beginning with a CT-scan. In the study HCC surveillance will be offered to all patients with compensated non-viral cirrhosis residing in the Central Denmark Region, one of five administrative regions of Denmark. The study aims to determine the efficacy of HCC surveillance in reducing HCC-related mortality by comparing HCC-related mortality between the Central Denmark Region and the other four Danish regions, where HCC surveillance is not offered.

This description comes directly from the study's public registry record.

Talk to the study team

Peter Jepsen, Professor, MD, PhD  ·  +45 29314466  ·  pj@clin.au.dk

Morten Hallengreen, PhD student  ·  +45 60154398  ·  mohall@clin.au.dk

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Cirrhosis * No history of chronic hepatitis B or C * Compensated cirrhosis defined as: * No recent variceal bleeding, no uncontrolled ascites, no clinically apparent hepatic encephalopathy, and Child-Pugh score ≤ 8 * Age 40-79 years * Expected remaining life expectancy ≥ 1 year * Not already in follow-up after treatment for HCC * No clinical suspicion of HCC Exclusion Criteria: \-

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (6)

Aarhus University HospitalAarhus, Central Jutland, DenmarkRecruiting
Regional Hospital GødstrupHerning, Central Jutland, DenmarkRecruiting
Horsens Regional HospitalHorsens, Central Jutland, DenmarkRecruiting
Randers Regional HospitalRanders, Central Jutland, DenmarkRecruiting
Silkeborg Regional HospitalSilkeborg, Central Jutland, DenmarkRecruiting
Viborg Regional HospitalViborg, Central Jutland, DenmarkRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

AarhusHerningHorsensRanders

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