Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06923176

Effect of Biejia-Ruangan Compound on Survival Rate and Recurrence Rate of Hepatocellular Carcinoma After Radical Treatment

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
704 (estimated)
Sponsor
Zhiyun Yang · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study plans to enroll 704 patients with a history of chronic hepatitis B who have undergone radical treatment for hepatocellular carcinoma. The subjects were divided into a control group (conventional treatment group) and a combination therapy group (conventional treatment plus Biejia-Ruangan compound) according to the doctor's clinical diagnosis and treatment and the subjects' wishes in a ratio of 1:2. The subjects in the combination therapy group were treated with Biejia-Ruangan compound for 72 weeks, followed by 168 weeks of follow-up, for a total study period of 240 weeks. By analyzing the 1-, 2-, 3-, and 5-year recurrence-free, overall survival rate/survival time, adverse reactions, etc., the clinical effect of Biejia-Ruangan compound in reducing the risk of recurrence in patients with hepatocellular carcinoma after receiving radical treatment was comprehensively evaluated, and its scientific value and practical application prospects as a potential treatment method were explored.

Conditions

Interventions

TypeNameDescription
DRUGBiejia-Ruangan compoundBiejia-Ruangan compound have the functions of softening hardness, dispersing lumps, removing blood stasis and detoxifying, and nourishing qi and blood. Used for chronic hepatitis B liver fibrosis, as well as early liver cirrhosis characterized by blood stasis obstructing collaterals, qi and blood deficiency with incomplete heat toxicity.
OTHERRoutine medical careRoutine medical care

Timeline

Start date
2025-04-19
Primary completion
2031-04-30
Completion
2031-04-30
First posted
2025-04-11
Last updated
2025-04-11

Source: ClinicalTrials.gov record NCT06923176. Inclusion in this directory is not an endorsement.