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

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

DETECT-HCC-ESLD is a prospective multicenter study designed to examine early detection and risk stratification of hepatocellular carcinoma (HCC) in individuals with advanced liver disease. Adults with cirrhosis of different etiologies are enrolled and followed longitudinally with structured clinical assessments and imaging at predefined intervals. A key objective is to evaluate ultrasound and abbreviated MRI (AMRI) as surveillance modalities for HCC. The study examines detection performance, feasibility, and factors influencing image quality and interpretability. The protocol also includes the study of body composition, focusing on how variations in adiposity and muscle mass may relate to imaging characteristics, disease progression, and HCC risk. Longitudinal clinical and imaging data are used to explore prediction models aimed at identifying patients with differing levels of HCC risk. The study records outcomes such as incident HCC, liver-related complications, and mortality to support analyses of disease trajectories. The DETECT-HCC-ESLD study provides a structured framework for collecting clinical, imaging, and body composition data over time, enabling detailed evaluation of surveillance strategies and risk patterns in advanced liver disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Sweden
Department of gastroenterology and hepatology, University hospital in Linköping
RECRUITING
Linköping
Contact Information
Primary
Mattias Ekstedt, MD, PhD
mattias.ekstedt@liu.se
0046709296267
Time Frame
Start Date: 2025-12-18
Estimated Completion Date: 2031-12
Participants
Target number of participants: 600
Treatments
Adult patients with liver cirrhosis without prior hepatocellular carcinoma
Sponsors
Collaborators: Västra Götalandsregionen, Uppsala County Council, Sweden, Amra Medical AB, Region Stockholm, Region Östergötland, Region Jönköping County, Örebro County Council, Norrlands Universitetssjukhus, Umea, Sweden, Antaros Medical
Leads: Mattias Ekstedt

This content was sourced from clinicaltrials.gov