Skip to main content
Clinical Trials/NCT02826005
NCT02826005
Unknown
Not Applicable

Examination the Ability to Early Diagnose HCC

Ilex Medical0 sites400 target enrollmentJuly 2016
ConditionsFibrosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fibrosis
Sponsor
Ilex Medical
Enrollment
400
Primary Endpoint
Diagnosis of HCC in cirrhotic patients with positive values of the bio-markers by MRI
Last Updated
9 years ago

Overview

Brief Summary

Examination the ability to early diagnose HCC by combining three biomarkers technology developed by WAKO, And their relevance to cirrhotic of patients with various backgrounds and the Israeli population.

This blood test will serve as an additional diagnostic tool tools currently in use (Ultrasound and AFP levels) to cirrhotic patients with high risk to develop hepatocellular carcinoma.

Another group that will be examined for all three biomarkers will be patients which already diagnosed with hepatocellular carcinoma, and have normal AFP level in order to examine the correlation between the presence of tumor, the number of them and the tumor size and the three biomarkers concentration in their blood

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
August 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ilex Medical
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients with chronic liver disease or cirrhotic or with diagnoses HCC with HCV, HBV, NAFLD, Alcohol background

Exclusion Criteria

  • patients with chronic liver disease or cirrhotic or with diagnoses HCC with autoimmune background or other background than HCV, HBV, NAFLD and Alcohol.

Outcomes

Primary Outcomes

Diagnosis of HCC in cirrhotic patients with positive values of the bio-markers by MRI

Time Frame: within 3 years from the bio-markers examination

Similar Trials