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Study identifier: NCT06658782 Synced from ClinicalTrials.gov · July 29, 2026
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Abbreviated Magnetic Resonance Imaging vs Ultrasound Surveillance for Liver Cancer dETection in People at High Risk of Developing Liver Cancer

Condition: Cirrhosis · Cirrhosis Due to Hepatitis B · Cirrhosis and Chronic Liver Disease  ·  Sponsor: University of Oxford

PhaseN/A
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Aim: To use magnetic resonance imaging (MRI) scans without contrast to help improve diagnosis of liver cancer in people who are at increased risk of developing liver cancer. Background: People with any condition that affects the liver over a long period of time can develop cirrhosis. Conditions and risk factors that can lead to cirrhosis include alcohol excess, liver steatosis (lipid or fat accumulation in the liver) and infection with the viruses hepatitis B and C. One of the concerns about people with cirrhosis is that they are at increased risk of developing liver cancer. People with cirrhosis are recommended to have an ultrasound scan (USS) every 6 months (surveillance for liver cancer) so that if a cancer develops, it is diagnosed at an early stage when it can be cured. However, ultrasound can miss cancers even in people having scans every 6 months. Furthermore, the risk of cancer is not alike among people with cirrhosis. For example, people with more advanced cirrhosis and those with cirrhosis from hepatitis B are at higher risk. It is therefore possible that better tests than ultrasound are needed for people with cirrhosis who are at particularly high risk of developing cancer. Computed tomography (CT) and Magnetic Resonance Imaging (MRI) scans with dye injection (contrast) are used for liver cancer diagnosis. However, they cannot be done every 6 months because of costs, capacity and toxicity from high CT radiation doses, and MRI contrast build-up in the brain with r…

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

Talk to the study team

Michael Pavlides, DPhil  ·  +44 1865234577  ·  michael.pavlides@cardiov.ox.ac.uk

Always discuss trial participation with your own doctor first.

Locations (2)

Oxford University Hospitals NHS Foundation TrudtOxford, Oxon, United KingdomRecruiting
Bournemouth University HospitalBournemouth, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06658782