About this trial
This study aims to establish a prospective, multicenter, randomized, double-blind, placebo-controlled parallel-group clinical trial cohort. The cohort will include high-risk populations for hepatitis B cirrhosis-related hepatocellular carcinoma (HCC) from multiple centers nationwide, who meet the criteria of traditional Chinese medicine syndrome differentiation as Qi-zhi-xue\_yu syndrome and have an aMAP score \>60 points. The objective is to evaluate whether combining Bie-jia-ruan-gan with standard anti-hepatitis B virus therapy can further reduce the incidence of HCC in this high-risk population.
Eligibility criteria
Qualifiers
Voluntarily signed informed consent form
Aged 18-65 years
Traditional Chinese Medicine (TCM) syndrome type: Qi-zhi -xue-yu
Meeting the diagnostic criteria for hepatitis B-related cirrhosis
Disqualifiers
[Previously diagnosed with or treated for hepatocellular carcinoma (HCC) or other malignancies
Pregnant or lactating women
Decompensated cirrhosis (e.g., presence of obvious ascites, hepatic encephalopathy, or gastrointestinal bleeding)
Concomitant liver diseases, including but not limited to hepatitis C virus infection, human immunodeficiency virus infection, alcoholic liver disease, autoimmune liver disease, or drug-induced liver injury
Trial design
Treatments tested in this trial
- Biejia-Ruangan compound
- Biejia-Ruangan compound simulant
Treatment groups
Locations
Sponsors and collaborators
Nanfang Hospital, Southern Medical University
Lead sponsor
Shenzhen Third People's Hospital
Collaborator
Beijing Ditan Hospital
Collaborator
Beijing 302 Hospital
Collaborator