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UnknownNCT02826005

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.

Examination the Ability to Early Diagnose HCC

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
Ilex Medical · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DEVICEMRI

Timeline

Start date
2016-07-01
Primary completion
2017-08-01
Completion
2017-08-01
First posted
2016-07-07
Last updated
2016-07-12

Source: ClinicalTrials.gov record NCT02826005. Inclusion in this directory is not an endorsement.

Examination the Ability to Early Diagnose HCC by Combining Three Biomarkers Technology Developed by WAKO, And Their Rele (NCT02826005) · Clinical Trials Directory