ClinicalTrials.Veeva

Menu

Predictive Power of Share Wave Fibro Scan in HCC After HCV Infection

A

Assiut University

Status

Completed

Conditions

Hepatocellular Carcinoma

Treatments

Diagnostic Test: Share wave fibro scan

Study type

Observational

Funder types

Other

Identifiers

NCT05105828
Share wave fibro scan in HCC

Details and patient eligibility

About

Shear wave electrography score allows stratification of HCC risk in a noninvasive and reliable way and can guide the surveillance strategy for HCC in patients with CLD

Full description

Liver fibrosis is common to all chronic liver disease (CLD) , With time, this progressive disruption of hepatic architecture can develop into cirrhosis, characterized by "diffuse conversion of normal liver architecture into structurally abnormal nodules", About1% to 4% of patients with HCV-induced liver cirrhosis are diagnosed with HCC each year .

The historical gold standard for quantifying fibrosis is liver biopsy, but its invasive nature and potential for complications make it unpopular among patients and impractical for serial assessments of CLD. Furthermore, since histological lesions are not uniformly distributed across the liver parenchyma, this allows for large sampling error. The need for credible alternatives to biopsy has stimulated research into non-invasive methods of fibrosis assessment, including serum biomarkers , axial imaging and transient elastography.

FibroScan™ (Echosens, Paris, France) allows a non-invasive liver stiffness measurement (LSM), it is a relatively simple, highly reproducible and operator independent technique which examines an area 100 times that of a biopsy, reducing sampling bias , Shear wave elastography (SWE) measures LS by quantifying the velocity of shear waves produced in the liver tissue and uses a normal B-mode ultrasound probe for measuring LS in real time. In addition, SWE imaging using the Aixplorer system provides a high frame-rate and may be able to provide more accurate scoring of fibrosis .

Enrollment

110 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Post hepatitis C with HCC

Exclusion criteria

  • hepatic encephalopathy, ascites or pregnancy, hepatorenal syndrome or hepato-pulmonary syndrome, right side heart failure (liver congestion), extra hepatic tumors, history of liver transplantation, cholestasis, and hepatitis B patient

Trial design

110 participants in 2 patient groups

post Hepatitis C patients with hepatocellular carcinoma
Description:
post Hepatitis C patients with hepatocellular carcinoma above 18 years
Treatment:
Diagnostic Test: Share wave fibro scan
control group
Description:
post Hepatitis C patients without hepatocellular carcinoma above 18 years
Treatment:
Diagnostic Test: Share wave fibro scan

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems