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Clinical Trial Summary

De-identified whole blood and serum samples are collected for the purpose of evaluating the performance (sensitivity/specificity) of the HelioLiver Test for the detection of hepatocellular carcinoma (HCC).


Clinical Trial Description

The purpose of this study is to define the performance characteristics (sensitivity and specificity) of the Helio Liver Test within a study population of subjects that have been diagnosed with liver cancer at various stages (I to IV) and for control subjects who have been confirmed to not have liver cancer by at least one imaging technique, such as ultrasound, MRI or CT. Control subjects will include patients who are at high-risk for liver cancer and have been recommended to undergo liver cancer surveillance. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05053412
Study type Observational
Source Helio Genomics
Contact
Status Enrolling by invitation
Phase
Start date September 1, 2021
Completion date June 30, 2024