Improving screening for liver cancer
Official title: Prospective Comparison of Diagnostic Performance and Cost-effectiveness of US and Abbreviated MRI for Hepatocellular Carcinoma Screening
Run by University of Lausanne Hospitals · NCT05828446 · Data updated 2026-11-12
This study is testing whether a special type of MRI can find liver cancer better than regular ultrasound in people with chronic liver disease.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 330 (estimated) |
| Sponsor | University of Lausanne Hospitals Academic / other |
| Locations | 1 site (Lausanne, Canton of Vaud) |
| Status | Recruiting |
| Started | April 1, 2023 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | November 2, 2026 |
| Trial ID | NCT05828446 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with chronic liver disease who require HCC screening as per established guidelines.
✕Probably not a fit
Patients with a history of HCC, other malignancies, or those unsuitable for MRI will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study aims to compare the effectiveness of ultrasound versus abbreviated magnetic resonance imaging (AMRI) in detecting hepatocellular carcinoma (HCC) in patients with chronic liver disease. Participants will undergo screening rounds that include both ultrasound and MRI within the same week, conducted bi-annually. The study hypothesizes that AMRI with a contrast agent will yield a higher detection rate of HCC compared to routine ultrasound screenings.
Why it matters
Potential benefit: If successful, this study could lead to improved early detection of liver cancer, potentially enhancing patient outcomes.
How similar studies have gone: While this approach is innovative, similar studies have shown promise in improving cancer detection rates using advanced imaging techniques.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All adult patients with chronic liver disease and indication for HCC screening according to the European Association for the Study of the Liver recommendations. * Informed Consent signed by the subject Exclusion Criteria: * History of HCC * History of other malignancy * Prior liver nodule categorized as LI-RAD 4, 5 or M * History of liver transplantation * Pregnancy * MRI or MRI contrast agent precaution * Any other condition making the patient unsuitable for the study * Patient's refusal of transmission of relevant medical conditions found on the medical examinations performed during the study
Where it's running
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Lausanne University Hospital
Lausanne, Canton of Vaud, Switzerland Recruiting
Study contacts
- Principal investigator: Naik Vietti Violi, MD — University of Lausanne Hospitals
- Study coordinator: Naik Vietti Violi, MD
- Email: naik.vietti-violi@chuv.ch
- Phone: +41213144556
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.