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Clinical Trials/NCT06777485
NCT06777485
Recruiting
Not Applicable

China Liver Cancer Clinical Registry Cohort Database (HEAL)

Anhui Provincial Hospital38 sites in 1 country10,000 target enrollmentJanuary 1, 2025

Overview

Phase
Not Applicable
Intervention
Procedure/Surgery treatment
Conditions
Not specified
Sponsor
Anhui Provincial Hospital
Enrollment
10000
Locations
38
Primary Endpoint
OS
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

This study was led by the Department of Hepatobiliary Surgery of the First Affiliated Hospital of the University of Science and Technology of China (USTC), in close cooperation with many participating units across the country, to establish a standardized clinical information database of hepatocellular carcinoma cohorts, which will provide a guarantee for conducting high-quality real-world clinical studies and clinical research.

Registry
clinicaltrials.gov
Start Date
January 1, 2025
End Date
January 1, 2035
Last Updated
8 months ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Anhui Provincial Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years, no gender limit
  • Patients without surgery are initially diagnosed with hepatocellular carcinoma, intrahepatic cholangiocarcinoma, mixed hepatocellular carcinoma-cholangiocarcinoma, or metastatic hepatocellular carcinoma based on the results of imaging and laboratory tests, or patients with surgery are diagnosed with hepatocellular carcinoma, intrahepatic cholangiocarcinoma, mixed hepatocellular carcinoma-cholangiocarcinoma, or metastatic hepatocellular carcinoma based on the results of pathologic tests
  • Signed informed consent, good compliance, willingness to accept follow-up and provide blood and postoperative pathology residual samples

Exclusion Criteria

  • Combination of severe central nervous system disease, respiratory disease, autoimmune disease, chronic renal insufficiency, long-term use of immunosuppressive drugs, combination of severe uncontrolled infections
  • Concurrent active cardiovascular disease, cerebrovascular accident within 6 months, myocardial infarction, unstable angina pectoris, or congestive heart failure of class II or greater according to the New York Heart Association criteria, severe arrhythmia requiring medication
  • Pregnant or breastfeeding women
  • Participation in other therapeutic clinical trials during the course of the patient's illness in which the treatment cannot be specified or information about the treatment cannot be collected

Arms & Interventions

Liver Cancer

Observation of clinical routine treatment in patients with Liver cancer

Intervention: Procedure/Surgery treatment

Liver Cancer

Observation of clinical routine treatment in patients with Liver cancer

Intervention: Anti-Tumor Drugs

Outcomes

Primary Outcomes

OS

Time Frame: 10 years

Time from enrollment to first recorded occurrence of death from any cause

Secondary Outcomes

  • RFS(10 years)
  • Survival time after recurrence(10 years)

Study Sites (38)

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