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临床试验/JPRN-UMIN000016256
JPRN-UMIN000016256已完成未知

A phase II study of capecitabin plus oxaliplatin therapy (XELOX) for inoperable/advanced gastric cancer resistant/intolerable to fluoro-pyrimidine, CDDP, Taxane or CPT-11 (OGSG1403) - A phase II study of capecitabin plus oxaliplatin therapy (XELOX) for inoperable/advanced gastric cancer resistant/intolerable to fluoro-pyrimidine, CDDP, Taxane or CPT-11 (OGSG1403)

Osaka Gastrointestinal Cancer Chemotherapy Study Group (OGSG)0 个研究点目标入组 12 人开始时间: 2015年1月19日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
12

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)With prior chemotherapy including oxaliplatin (L-OHP) 2)With some active double cancers 3)With severe complications 4)With active infectious diseases which need treatments 5)With thoracic fluid and/or ascites which need drainage 6)under continuous steroids medication 7)under medication of phenytoin and/or warfarin 8)with active bleeding which needs frequent blood transfusion 9)with central nerve metastases with symptoms 10) with psychological disorders 11) Pregnant and/or nursing women or men who like to have children 12)Any other patients whom the physician in charge of the study judges to be unsuitable

研究者

发起方
Osaka Gastrointestinal Cancer Chemotherapy Study Group (OGSG)

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