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NCT05828446Recruiting

Improving Hepatocellular Carcinoma Screening

Prospective Comparison of Diagnostic Performance and Cost-effectiveness of US and Abbreviated MRI for Hepatocellular Carcinoma Screening

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

This is a monocentric, single blind, interventional, single arm study. It is designed to compare the rates of detection of hepatocellular carcinoma (HCC) by ultrasound (US) used in clinical routine vs. abbreviated magnetic resonance imaging (AMRI). The hypothesis is that dynamic AMRI with extracellular contrast agent injection has a higher patient-level detection rate of HCC than screening US and non-contrast AMRI. Interested and eligible patients will be enrolled and undergo HCC screening rounds including US +/- contrast-enhanced US (clinical routine) and screening MRI within the same week bi-annually.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
330 (estimated)
First submitted
19 Jan 2023
Start date
1 Apr 2023
Primary completion date
31 Dec 2027
Lead sponsor
Naik Vietti Violi
NCT number
NCT05828446

What you commit to

  • Study type: Interventional
  • Planned participants: 330
  • From 1 Apr 2023 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior liver nodule categorized as LI-RAD 4, 5 or M

Other illness

  • History of HCC
  • History of other malignancy
  • History of liver transplantation
  • 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

Other

  • Pregnancy
  • MRI or MRI contrast agent precaution

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lausanne University Hospital
Coordinator of this site? Confirm its status
LausanneSwitzerlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.