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临床试验/JPRN-UMIN000012041
JPRN-UMIN000012041已完成2 期

Efficacy of postoperative hepatic arterial infusion chemotherapy with CDDP for hepatocellular carcioma with early recurrence risk factors. - adjubant CDDP TAI for HCC with high recurrence risk factors.

Department of Gastroenterology and Metabolism,Hiroshima University Hospital0 个研究点目标入组 60 人开始时间: 2013年10月15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
60

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 85years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with mixed hepatocellular and cholangiocellular carcinoma diagnosed by histologial examination 2) Severe arterio-portal or arterio-venous shunts in the liver 3) Patinets with difficulty with drug arrival to hepatic lesion 4) Other uncontrolled severe illness a. With severe cardiac failure b. With severe renal function disease c. With active infectious disease except viral hepatitis d. With active gastrointestinal hemorrhage e. With active other malignancies f. With hepatic encephalopathy and severe mental disorder g. With clinically significant refractory ascites or pleural effusion 5) Allergic reaction to iodine contrast material, gadolinium contrast material, or platium containing agent. 6)Patients medicated with steroid 7) A pregnant woman, or a woman suspected of pregnancy. 8) Patients who are concluded to be inappropriate to participate in this study by their physitians

研究者

发起方
Department of Gastroenterology and Metabolism,Hiroshima University Hospital

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