Hepatic Carcinoma Clinical Trial
Official title:
A Multicenter, Randomized, Paralleled Control Clinical Study Investigating Huaier Granule for Prevention of Recurrence and Metastasis of Hepatocarcinoma After Radical Hepatectomy
Verified date | March 2017 |
Source | Qidong Gaitianli Medicines Co., Ltd |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To evaluate the efficacy and safety of Huaier Granule for prevention of recurrence and metastasis of hepatocarcinoma after radical hepatectomy.
Status | Completed |
Enrollment | 1044 |
Est. completion date | August 2016 |
Est. primary completion date | August 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Age: = 18 and = 75 years, both male and female; - Radical hepatectomy has been performed for hepatocellular carcinoma; - The hepatocellular carcinoma has been confirmed by pathological examination; - Barcelona clinic liver cancer(BCLC) stage A or B; - Not receiving any preoperative anticancer drug; - The liver and kidney function satisfies the following conditions within 15 days after surgery (excluding day 15): aspartate aminotransferase(AST), glutamic-oxalacetic transaminase(ALT)<3 upper limit of normal(ULN), total bilirubin=2ULN, serum creatinine <1.5 ULN; - Other laboratory tests meet the following requirements within 15 days after surgery (excluding day 15): Hb=9g/dl, platelet count=60×109/L, absolute neutrophil count>1.0×109/L; - The expected survival time = 12 weeks; - The subjects volunteer to sign the informed consent. Exclusion Criteria: - Hepatocellular carcinoma patients who received non-radical hepatectomy; - Non-hepatocellular carcinoma patients; - Those with Child-Pugh C; - Pregnant or lactating women; - Those with active bleeding due to various reasons; - Those with HIV infection or AIDS-associated diseases; - Those with severe acute and chronic diseases; - Those with severe diabetes; - Those with serious infectious diseases; - Those who can not take drugs by oral route; - Drug abusers or those with psychological or mental diseases that may interfere with study compliance; - Conditions that are considered not suitable for this study investigators |
Country | Name | City | State |
---|---|---|---|
China | Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology | Wuhan | Hubei |
Lead Sponsor | Collaborator |
---|---|
Qidong Gaitianli Medicines Co., Ltd | Huazhong University of Science and Technology |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of Recurrence and Metastasis After Hepatectomy | At week 94 after took medicine, assess incidence of recurrence and metastasis after hepatectomy. | Week 94 after took medicine | |
Secondary | Postoperative Survival Period | Assess Postoperative survival period | Week 94 after took medicine |
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