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Study identifier: NCT05095714 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

FAST-IRM for HCC suRveillance in pAtients With High risK of Liver Cancer.

Condition: Hepatocellular Carcinoma · Liver Cancer · Cirrhosis  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants944
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Intro: Hepatocellular carcinoma (HCC) is the 6th leading cause of cancer worldwide. In France, more than 10,000 new cases are identified each year. The latter occur in 85% of cases in cirrhosis, the most frequent causes of which are excessive alcohol consumption, metabolic syndrome or HBV/HCV infection. Patients with cirrhosis justify being included in monitoring programs involving the performance of a semi-annual liver ultrasound (US) in order to detect HCC eligible for curative treatment (liver resection or percutaneous ablation). This practice is considered to be cost-effective in the event of an annual incidence of HCC\> 1.5%. US in this context has a low sensitivity for the detection of HCC at the very early stage and the following observations have been made in the last 20 years: * The rate of patients detected at early stage BCLC 0 is around 30% by ultrasound * The rate of patients included in surveillance programs detected with advanced HCC eligible for palliative treatment is around 20% * Reducing the periodicity of liver ultrasounds from 6 to 3 months does not improve these results. In parallel, liver MRI has been evaluated as a tool for the early detection of HCC. Its performance for the detection of HCC at the very early stage exceeds 80%. However, due to the higher cost compared to US, it was estimated that its use in screening context would only be cost effective in the event of an annual incidence\> 3%. In addition, the practice of these expensive and long-la…

This description comes directly from the study's public registry record.

Talk to the study team

Pierre NAHON, MD, PhD  ·  1 48 02 62 80  ·  pierre.nahon@aphp.fr

David SCHMITZ  ·  1 49 81 36 32  ·  david.schmitz@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Assistance Publique Hôpitaux de Paris - Hôpital AvicenneBondy, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05095714