Last updated: May 14, 2026
Sponsor: The University of Hong Kong
Overall Status: Completed
Phase
N/A
Condition
Carcinoma
Liver Cancer
Abdominal Cancer
Treatment
LI-RADS
Prototype artificial intelligence algorithm
Clinical Study ID
NCT06626087
HMRF HCC AI
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age >=18 years.
- Defined as the at-risk population requiring regular liver ultrasonographysurveillance.
These include:
Cirrhotic patients of any disease etiology,
Chronic hepatitis B patients of age ≥40 years for men, age ≥50 years for women orwith a family history of HCC.
- At least one new-onset focal liver nodule detected on liver ultrasonography.
Exclusion
Exclusion Criteria:
- Liver nodules of <1 cm. Currently such nodules are not reported using LI-RADScriteria but are recommended for a repeat scan in 3-6 months. In patients withmultiple liver nodules, the largest nodule will be assessed.
- Patients with contraindications for contrast CT imaging, including a history ofcontrast anaphylaxis and impaired renal function (glomerular filtration rate <30ml/min).
- Patients with prior transarterial chemoembolization or other interventionalprocedures with intrahepatic injection of lipiodol. Lipiodol is extremely hyperdenseon computed tomography and will preclude objective interpretation. Such patientswere also excluded in the development of our prototype AI algorithm.
Study Design
Total Participants: 300
Treatment Group(s): 2
Primary Treatment: LI-RADS
Phase:
Study Start date:
November 01, 2023
Estimated Completion Date:
March 31, 2026
Study Description
Connect with a study center
Department of Medicine and Department of Surgery, The University of Hong Kong, Queen Mary Hospital
Hong Kong,
Hong KongSite Not Available
Department of Medicine, The University of Hong Kong, Queen Mary Hospital
Hong Kong,
Hong KongSite Not Available

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