Clinical Trial

Fibroscan Evaluating Immunotherapy Response in Hepatocellular Carcinoma

Recruiting
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Record status
This record was last updated May 7, 2025 (before its estimated January 15, 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of this prospective cohort study is to evaluate the role of transient elastography (Fibroscan) in predicting the response of immunotherapy in advanced Hepatocellular carcinoma (HCC) patients. Researchers will predict the response to 6 months of HCC immunotherapy regarding improvement of the degree of liver fibrosis, development of liver decompensation, complications, survival, and mortality. Participants will undergo history-taking, clinical examination, laboratory investigations, Child-Pugh classification, Model for End-stage Liver Disease (MELD) score, BCLC staging, abdominal ultrasonography, Triphasic CT abdomen with contrast or MRI (for evaluation of tumor site, size and number), and Fibroscan examination at baseline and follow-up after 6 months.
Trial Details
NCT Number NCT06960863
Lead Sponsor Tanta University
Conditions Hepato Cellular Carcinoma (HCC)
Enrollment 80 participants
Start Date 2025-01-26
Primary Completion 2026-01-15 (estimated)
Study Completion 2026-01-31 (estimated)
Updated on ClinicalTrials.gov 2025-05-07