跳至主要内容
临床试验/JPRN-UMIN000007473
JPRN-UMIN000007473招募中未知

PhaseI/II study of TS-1+CDDP in combination with Radiotherapy with unresectable and locally advanced for biliary tract cancer - PhaseI/II study of TS-1+CDDP in combination with Radiotherapy with unresectable and locally advanced for biliary tract cancer

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University0 个研究点目标入组 25 人开始时间: 2012年3月8日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
25

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) severe drug allergy (10) pregnant women or during the nursing, women who like be pregnant and willing to get pregnant, men who want his partner to be pregnant (11) doctor's decision not to be registered to this study

研究者

发起方
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University

相似试验