Skip to content

Cohort Establishment and Translation of Hepatocellular Carcinoma in the Context of Metabolic Dysfunction-Associated Steatotic Liver Disease

Cohort Establishment and Translation of Hepatocellular Carcinoma in the Context of Metabolic Dysfunction-Associated Steatotic Liver Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110623
Enrollment
Unknown
Registered
2025-10-16
Start date
2025-10-16
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Metabolic Dysfunction-Associated Steatotic Liver Disease related Hepatocellular Carcinoma

Interventions

Observation group:None

Sponsors

the First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. Hepatic steatosis confirmed by radiology (abdominal ultrasound, CT, MRI, CAP >= 248 dB/m, or MRI-PDFF or MRS hepatic fat fraction >= 5%) or histology (fatty change involving >= 5% of hepatocytes) and HCC diagnosis; 3. At least one cardiometabolic risk factor (overweight/obesity, abnormal blood glucose or type 2 diabetes, dyslipidemia, abnormal HDL cholesterol, abnormal blood pressure); 4. Clinical outcomes can be determined through medical record review or a reliable database.

Exclusion criteria

Exclusion criteria: 1. Evidence of other liver diseases such as positive hepatitis B surface antigen or alcoholic liver disease at baseline or during follow-up; 2. Positive hepatitis C virus antibody (unless HCV RNA is negative and untreated, or SVR achieved >=3 years prior to baseline MRI); 3. HIV infection at baseline or during follow-up; 4. Secondary causes of fatty liver (such as use of systemic steroids, tamoxifen, or methotrexate); 5. History of other malignant tumors at baseline; 6. History of other malignant tumors before baseline (unless remission =5 years).

Design outcomes

Primary

MeasureTime frame
Ovall Survival;Recurrence-free Survival;

Countries

China

Contacts

Public ContactMinghua Zheng

the First Affiliated Hospital of Wenzhou Medical University

zhengmh@wmu.edu.cn+86 139 6778 1644

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026