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临床试验/JPRN-UMIN000008571
JPRN-UMIN000008571已完成2 期

Phase II study of weekly fractionated hepatic arterial infusion of Sorafenib and Cisplatin for advanced hepatocellular carcinoma. - Phase II study of weekly fractionated hepatic arterial infusion of Sorafenib and CDDP for advanced

Kansai Medical University Hirakata Hospital0 个研究点目标入组 33 人开始时间: 2012年7月31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
33

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 90years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Presence of metastasis 2.Presence of hepatic encephalopathy 3.Patients with active bacterial infection 4.Patients having blood vessel abnormality that difficult to insert hepatic arterial infusion port 5.Patients having severe disease 6.Patients losing of control over bowel movements 7.Patients with double cance 8.During pregnancy or breast-feeding woman 9.Contraindication of sorafenib or cisplatin

研究者

发起方
Kansai Medical University Hirakata Hospital

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