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A longitudinal 5-year study for the prediction of HCC, death and liver decompensation by ARFI elastography

Conditions
K74.0
Hepatic fibrosis
Registration Number
DRKS00031824
Lead Sponsor
Medizinische Klinik 1, Universitätsklinikum Erlangen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
335
Inclusion Criteria

Correct ARFI measurement (at least 5 measurements) of the right liver lobe, follow-up patient data of at least 5 years after ARFI measurement

Exclusion Criteria

Inadequate ARFI measurement, no complete follow-up data during the observation period

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver related survival
Secondary Outcome Measures
NameTimeMethod
Overall survival, occurrence of HCC, occurrence of liver decompensation/variceal bleeding
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