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临床试验/JPRN-UMIN000009028
JPRN-UMIN000009028已完成1 期

PhaseI/II study of neoadjuvant TS-1+CDDP with concurrent radiation for biliary tract cancer - PhaseI/II study of neoadjuvant TS-1+CDDP with concurrent radiation for biliary tract cancer

Keio University School of Medicine0 个研究点目标入组 40 人开始时间: 2012年10月5日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
40

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 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)bowel movement control is difficult, because of watery diarrhea and chronic diarrhea. (2)administered flucytosine, Phenytoin, Warfarin potassium (3)Pleural effusion or ascitic fluid accumulates (4)with clinically important infection (5)has active carcinoma except carcinoma in situ (6)with gastrointestinal active ulcer (7)sever complication(Heart failure, renal failure,liver failure,Intestinal paralysis,uncontrollable diabetes etc) (8)severe mental disorder (9)pregnant women or during the nursing, women who like be pregnant and willing to get pregnant,men who want his partner to be pregnant (10)doctors decision not to be registered to this study

研究者

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