Clinical Trials Directory

Trials / Completed

CompletedNCT03767764

Yliver as a Test to Early Diagnose HCC

Yliver as a Test to Early Diagnose Hepatocellular Carcinoma

Status
Completed
Phase
Study type
Observational
Enrollment
190 (actual)
Sponsor
Corporacion Parc Tauli · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Accepted

Summary

Liver cancer (HCC) is the second cause of death related to cancer worldwide, with about 750,000 deaths from this cause in 2012. Although the early diagnosis of liver cancer increases the available treatment options, the methods currently used for screening are not sufficiently sensitive for this purpose. The investigators provide a high-performance and highly reliable in vitro platform that allows the identification and quantification of autoantibodies in serum for use as biomarkers of liver cancer, using an ELISA test (Yliver). The aim of the study is to demonstrate whether the Yliver test can be used as a biomarker for the early diagnosis of hepatocellular carcinoma with a collection of samples from 58 patients diagnosed with HCC, 42 cirrhosis, 40 normal controls and the inclusion of 25-50 patients with chronic liver disease without cirrhosis.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTTest YliverTest Yliver is used to detect autoantibodies against alpha fetoprotein in serum by an ELISA technique

Timeline

Start date
2018-12-27
Primary completion
2020-04-01
Completion
2020-09-01
First posted
2018-12-07
Last updated
2021-07-29

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT03767764. Inclusion in this directory is not an endorsement.