Chronic Hepatitis B Clinical Trial
Official title:
Assessment of Liver FIBROsis by Real-time Tissue ELASTography in Chronic Liver Disease
This is a multi-center cross-sectional study in which the Real-time Tissue Elastography® measurements will be collected prospectively from patients with chronic hepatitis B or C virus presenting for liver biopsy.
The aim of this study is to validate the diagnostic value of Real-time Tissue Elastography®
by comparison with liver histology, serum marker or FibroScan® in chronic hepatitis B or C
patients.Real-time Tissue Elastography®, biopsy and serum maker are performed.
If in the hospital they can perform FibroScan®, FobroScan® also be performed. The subjects
must be scheduled for liver biopsy either prior to treatment (treatment naïve) or, if
previously treated, they must have been off treatment for at least six months. The time
between the Real-time Tissue Elastography® , biopsy, blood sampling and FiroScan® must not
exceed four weeks.
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Time Perspective: Prospective
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