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Comparison of Hepatus and FibroScan for Evaluation of Fibrosis and Steatosis

Comparison of Hepatus and FibroScan for Evaluation of Fibrosis and Steatosis in Chronic Hepatitis B or NAFLD Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05786963
Enrollment
400
Registered
2023-03-28
Start date
2022-12-29
Completion date
2024-04-30
Last updated
2023-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Hepatitis b, Non-Alcoholic Fatty Liver Disease

Keywords

Chronic Hepatitis b, Non-alcoholic Fatty Liver Disease, Liver fibrosis/cirrhosis, Steatosis

Brief summary

Totals of 400 chronic hepatitis B or non-alcoholic fatty liver disease (NAFLD) patients with or without cirrhosis will be enrolled. Patients' clinical characteristics, including alanine aminotransferase, aspartic aminotransferase, total bilirubin, direct bilirubin, indirect bilirubin, triglyceride and total cholesterol, hepatitis B surface antigen, steatosis, and liver stiffness measurement will be collected. The consistence of liver fibrosis and steatosis assessment between Hepatus and FibroScan will be evaluated in this study.

Interventions

None listed

Sponsors

Beijing Friendship Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with or without cirrhosis diagnose as chronic hepatitis B or non-alcoholic fatty liver disease; * Age above 18 years; * Signature of informed consent.

Exclusion criteria

* Patients with HCV and/or other viral hepatitis, autoimmune liver disease, alcoholic liver disease, genetic liver disease or other chronic liver diseases; * Patients with decompensated cirrhosis; * Patients with serum total bilirubin level higher than 51 umol/L; * Patients with liver malignant lesion, hemangiomas, giant liver cysts and other liver lesions; * Patients with HIV infections; * Patients after liver transplantation or TIPS; * Pregnant women; * Patients with Budd-Chiari syndrome, chronic congestive heart failure, constrictive pericarditis or other liver congestion lesions.

Design outcomes

Primary

MeasureTime frameDescription
Consistency of liver stiffness and steatosis results in the same location between Hepatus in continuous measurement mode and FibroScan in single detection mode.1 to 3 yearsConsistency of liver stiffness and steatosis between Hepatus and FibroScan.

Secondary

MeasureTime frameDescription
Consistency of liver stiffness and steatosis results between Hepatus in continuous measurement mode and FibroScan in single detection mode through the respective localization methods.1 to 3 yearsThe localization method of Hepatus is the real-time two-dimensional image guiding system, which is manually location in FibroScan.
Consistency of liver stiffness and steatosis results between Hepatus and FibroScan in single detection mode.1 to 3 yearsThe localization methods include the respective localization methods in Hepatus and FibroScan, and manually locating.
Comparison of measurement performance in Hepatus under continuous detection mode and in FibroScan through single detection mode.1 to 3 yearsEvaluation of measurement performance includes the rate of successful detection, time taken for validated detection, stability of liver stiffness measurement and controlled attenuation parameter.

Countries

China

Contacts

Primary ContactHong You, Doctor
youhong30@sina.com86-010-63139019
Backup ContactShuyan Chen, Doctor
13552962655@163.com86-010-63138656

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026