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临床试验/JPRN-UMIN000005495
JPRN-UMIN000005495已完成2 期

Transcatheter arterial infusion chemotherapy using cisplatin powder and iodized-oil for advanced hepatocellular carcinoma: a phase 2 study - HCC-CDDP+Lipiodol-P2

Japan Society of Transcatheter Hepatic Arterial Embolization Clinical Reserch Group0 个研究点目标入组 35 人开始时间: 2011年4月25日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
35

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)History of previous treatment by platinum drugs. 2)Extrahepatic metastasis. 3)Advanced vascular or biliary invasion (Vp4,Vv3,B3,B4). 4)Sever arterio-portal shunt or arterio-venous shunt. 5)Difficult to perform transcatheter arterial chemotherapy. 6)History of the biliary tract reconstruction or treatment. 7)Patients with following severe complicating disease(except chronic hepatitis and liver cirrhosis). 1.Heart failure 2.Renal failure 3.Active infections(except viral hepatitis) 4.Active gastrointestinal bleeding 5.Active duplicative cancer 6.Hepatic encephalopathy or severe mental illness 8)Fever >= 38.0 degrees Celsius. 9)History of hypersensitivity to iodine-containing contrast agent, gadolinium-containing contrast agent, and platinum-containing drug. 10)Patients who are pregnant, lactating, suspected to be pregnant, or wish to become pregnant. 11)Patients who are concluded to be inappropriate to participate in this study by their physicians.

研究者

发起方
Japan Society of Transcatheter Hepatic Arterial Embolization Clinical Reserch Group

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