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A Study of HCC High Risk Group Using Two Surveillance Tools

HCC Clinical Trial

Official title:
A Prospective Cohort Study to Compare Contrast Enhanced Liver CT and Ultrasonography for Hepatocellular Carcinoma Surveillance in High-risk Group of HCC: Preliminary Study

Clinical Trial Summary

The purpose of this study is to compare sensitivity for hepatocellular carcinoma (HCC) of bi-annual ultrasonography and low dose computed tomography (LDCT) in patients at high risk of HCC.

Clinical Trial Description

Patients at high risk of HCC are recommended to undergo biannual surveillance using ultrasound. In this study, LDCT is performed in addition to biannual ultrasound surveillance in eligible patients to compare their sensitivity for HCC. Standard of reference would be follow-up imaging and/or gadoxetic acid-enhanced liver MRI. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02675920
Study type Observational
Source Seoul National University Hospital
Contact
Status Completed
Phase
Start date November 28, 2014
Completion date October 1, 2019
View Details
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