Clinical trial Recruiting at 1 site Observational Ages 18 and up

MRI versus ultrasound for early liver cancer detection, body composition, and decompensation risk in cirrhosis

Official title: A Comparative Study of MRI and Ultrasound for Detection of Primary Hepatocellular Carcinoma, Body Composition and Risk Factors for Decompensation in Liver Cirrhosis

Run by Linkoeping University · NCT07291141 · Data updated 2026-11-12

This project will test whether abbreviated MRI or ultrasound is better at finding early liver cancer and measuring muscle and fat in adults with cirrhosis.

More Ultrasound trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment600 (estimated)
SponsorLinkoeping University
Government
Locations1 site (Linköping, Select A State Or Province)
StatusRecruiting
StartedDecember 18, 2025
Main results expectedDecember 2029
Study endsDecember 2031
Registry record updatedDecember 19, 2025
Trial IDNCT07291141 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–84 with clinically diagnosed liver cirrhosis, no prior HCC or liver transplant, able to undergo MRI, and able to give informed consent are ideal candidates.

Probably not a fit

People with MRI contraindications, pregnancy, primary sclerosing cholangitis, vascular liver disease, congenital liver fibrosis, prior HCC, prior liver transplant, or inability to travel to the study site are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective multicenter cohort of adults with clinically diagnosed cirrhosis followed with scheduled clinical assessments and imaging over time. Participants undergo both ultrasound and abbreviated MRI (AMRI) at predefined intervals to compare detection performance and image quality. The protocol includes quantitative body composition analysis (muscle and adiposity) to explore links with imaging characteristics, disease progression, and HCC risk. Longitudinal clinical and imaging outcomes are used to develop and test prediction models for incident HCC, liver-related complications, and mortality.

Why it matters

Potential benefit: If successful, the approach could enable earlier detection of HCC and better risk stratification, allowing timelier treatment and more personalized surveillance for people with cirrhosis.

How similar studies have gone: Previous studies indicate abbreviated MRI can be more sensitive than ultrasound for HCC detection, but large prospective multicenter comparisons that also incorporate body composition and longitudinal risk modeling remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with liver cirrhosis, according to clinical practice. Based on criteria such as elastography, symptoms, biopsy, or radiology.
* Age ≥18 years ≤ 84
* Written informed consent from the participant

Exclusion Criteria:

* Contraindications for MRI (ferrrous material, claustrophobia)
* Pregnancy
* Diagnosis of primary sclerosing cholangitis (PSC)
* Vascular liver disease
* Congenital liver fibrosis
* Previous diagnosis of hepatic carcinoma (HCC)
* Previous liver transplant

Where it's running

  • Department of gastroenterology and hepatology, University hospital in Linköping
    Linköping, Select A State Or Province, Sweden
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.