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Starting soon Observational

Predictors of HCC in Post-HCV Cirrhotic Patients After SVR

NCT07097870 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-08
Last updated
2025-08-05

Condition(s) studied

HCC - Hepatocellular Carcinoma

Study summary

This study aims to identify clinical and laboratory factors that predict the occurrence of hepatocellular carcinoma (HCC) in Egyptian cirrhotic patients after achieving a sustained virologic response (SVR) to hepatitis C virus (HCV) treatment. This is a retrospective, two-center, case-control study that will include 132 cases and 264 controls. Variables to be analyzed include demographics, liver disease status, metabolic comorbidities, lifestyle factors, medications, as well as laboratory parameters and non-invasive scoring systems.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * for cases: 1. age ≥ 18 y; 2. HCV related cirrhosis; 3. SVR12 after DAA; 4. radiologic or histologic HCC diagnosis ≤30 Jun 2025 * for controls: As above plus, ≥36 months post SVR without HCC Exclusion Criteria: * for cases: 1. non HCV cirrhosis or combined HCV-HBV cirrhosis; 2. HCC \<6 months before SVR; 3. concomitant cholangiocarcinoma * for controls: Same as cases, plus, loss to follow up before 36 months

Primary outcome measure(s)

  • occurrence of hepatocellular carcinoma (HCC) — from SVR12 achievement to 6-9 years later (time of data collection)
    measure occurrence of HCC in post-HCV liver cirrhosis after achieving SVR, by comparing cases to controls

Trial sites (1)

FacilityCityRegionStatus
Faculty of Medicine, Sohag Univesity Sohag Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07097870 on ClinicalTrials.gov ↗ ← All trials in Egypt