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Not yet recruiting Not applicable NCT07544121

Effect of Babao Dan Capsule Combined With Antiviral Therapy on the Incidence of Hepatocellular Carcinoma in Patients With Hepatitis B-related Cirrhosis

No applicable phase (e.g. observational)
Conditions: HEPATITIS B CHRONIC Cirrhosis, Liver Hepatocellular Carcinoma (HCC)

Sponsor: Nanfang Hospital, Southern Medical University

trial.available_in: БГ
Overview
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 Shi-re-du-yun syndrome and have an aMAP score \>60 points. The objective is to evaluate whether combining Babao Dan Capsule with standard anti-hepatitis B virus therapy can further reduce the incidence of HCC in this high-risk population.
Who can participate
Inclusion Criteria: 1. Voluntarily signed informed consent form 2. Aged 18-65 years 3. Traditional Chinese Medicine (TCM) syndrome type of Shi-re-du-yun 4. Meeting the diagnostic criteria for hepatitis B-related cirrhosis 5. aMAP score \> 60 Exclusion Criteria: 1. Previously diagnosed with or treated for hepatocellular carcinoma (HCC) or other malignancies 2. Pregnant or lactating women 3. Decompensated cirrhosis (e.g., presence of obvious ascites, hepatic encephalopathy, or gastrointestinal bleeding) 4. 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 5. Severe cardiac, renal, respiratory, or hematopoietic system diseases 6. Determined by the investigator to be unsuitable for participation in this trial
Interventions
Babao Dan Capsule
DRUG
Babao Dan Capsule simulant
DRUG
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
01.04.2026
Completion date
30.11.2028
Registry ID
NCT07544121
Source
clinicaltrials.gov
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