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临床试验/NCT03843229
NCT03843229Unknown4 期

Clinical Trial of Cinobufacini Combined With Transarterial Chemoembolization (TACE) on Primary Liver Cancer

The First Affiliated Hospital of Dalian Medical University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2019年1月27日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
90
试验地点
1
主要终点
tumor size

研究概览

简要总结

The clinical trail of Cinobufacini combined with TACE on primary liver cancer.The trail is randomized controled.Patients are diagnosed primary liver cancer based on pathology or cell biology.They are randomized into 2 groups:both groups receive TACE.The treatment group receives Cinobufacini injection 20ml via hepatic artery during Transarterial Chemoembolization(TACE) operation , Cinobufacini injection 20ml+5% Glucose injection 500ml from the second day of TACE until 7th day, and Cinobufacini tablet 3 tablets Tid for 2 months..The control group only receives TACE.Mainly to study Cinobufacini leads to the influence of the immunologic function after TACE.Immunological examination and Blood biochemistry evaluation include the number ratio、activity and function of immune cell,the immune cell marker(CD3、CD4、CD8,etc),tumor marker(CEA、AFP),etc.Clinical evaluation includes image data(CT/MRI),drug toxicities,quality of life(QOL),etc.

详细描述

The clinical trail of Cinobufacini combined with TACE on primary liver cancer.The trail is randomized controled.Patients are diagnosed primary liver cancer based on pathology or cell biology.They are randomized into 2 groups:both groups receive TACE.The treatment group receives Cinobufacini injection 20ml via hepatic artery during Transarterial Chemoembolization(TACE) operation , Cinobufacini injection 20ml+5% Glucose injection 500ml from the second day of TACE until 7th day, and Cinobufacini tablet 3 tablets Tid for 2 months..The control group only receives TACE.Mainly to study Cinobufacini leads to the influence of the immunologic function after TACE.Immunological examination and Blood biochemistry evaluation include the number ratio、activity and function of immune cell,the immune cell marker(CD3、CD4、CD8,etc),tumor marker(CEA、AFP),etc.Clinical evaluation includes image data(CT/MRI),drug toxicities,quality of life(QOL),etc.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age:18-70 years.
  • male and female.
  • signed the informed consent form.
  • Diagnosis:Primary liver cancer diagnosed by imaging、cell and pathology report.
  • Eastern Cooperative Oncology Group (ECOG) :0-2;life expectancy more than 3 months.
  • Indication for TACE,no contraindication.
  • First time chemotherapy or at least 6 months after last chemotherapy and radiotherapy.
  • At least 8 weeks after last biotherapy.
  • Surgery:had not received transplantation surgery,at least 2 weeks after last major surgery.

排除标准

  • Chemotherapy is contraindicated.
  • Have the primary disease can cause the neuropathy.
  • A history of other malignant tumor in recent 5 years.
  • Less than 6 months after last chemotherapy or radiotherapy.
  • Less than 8 months after last.
  • Cinobufacini allergy.
  • Had received transplantation surgery ,less than 2 weeks after last major surgery.
  • Other researchers think is not suitable for this clinical trail.

研究组 & 干预措施

treatment group

Experimental

The treatment group receives Cinobufacini injection 20ml via hepatic artery during Transarterial Chemoembolization(TACE) operation , Cinobufacini injection 20ml+5% Glucose injection 500ml from the second day of TACE until 7th day, and Cinobufacini tablet 3 tablets Tid for 2 months.

干预措施: Cinobufacini injection (Drug)

treatment group

Experimental

The treatment group receives Cinobufacini injection 20ml via hepatic artery during Transarterial Chemoembolization(TACE) operation , Cinobufacini injection 20ml+5% Glucose injection 500ml from the second day of TACE until 7th day, and Cinobufacini tablet 3 tablets Tid for 2 months.

干预措施: Transarterial Chemoembolization(TACE) (Procedure)

treatment group

Experimental

The treatment group receives Cinobufacini injection 20ml via hepatic artery during Transarterial Chemoembolization(TACE) operation , Cinobufacini injection 20ml+5% Glucose injection 500ml from the second day of TACE until 7th day, and Cinobufacini tablet 3 tablets Tid for 2 months.

干预措施: cinobufacini tablet (Drug)

control group

Other

The control group only receives Transarterial Chemoembolization (TACE).

干预措施: Transarterial Chemoembolization(TACE) (Procedure)

结局指标

主要结局

tumor size

时间窗: the 8th week after TACE operation

次要结局

  • the number of CD4+T cell,CD8+T cell in blood(the 8th week after TACE operation)
  • Interleukin(IL)-2,Interleukin(IL)-4,Interleukin(IL)-6,tumor necrosis factor(TNF)-α,interferon(INF)-γ in blood(the 8th week after TACE operation)

研究者

发起方
The First Affiliated Hospital of Dalian Medical University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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