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Study identifier: NCT06960863 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Fibroscan Evaluating Immunotherapy Response in Hepatocellular Carcinoma

Condition: Hepato Cellular Carcinoma (HCC)  ·  Sponsor: Tanta University

PhaseN/A
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Rania M Elkafoury, MD  ·  +201004672358  ·  rania.elkafoury@med.tanta.edu.eg

Nabila A Elgazzar, MD  ·  00201288585733  ·  nabilaelgazzar@med.tanta.edu.eg

Always discuss trial participation with your own doctor first.

Locations (1)

Tanta University HospitalsTanta, Gharbyea, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT06960863