跳至主要内容
临床试验/JPRN-UMIN000013669
JPRN-UMIN000013669招募中2 期

A PhaseII study of XP(capecitabine plus cisplatin) combination therapy for HER2 negative advanced/recurrent gastric cancer - SGCSG G-04

SGCSG:Shimane Gstroenterological Vancer Study Group0 个研究点目标入组 36 人开始时间: 2014年4月8日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
36

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)Forbidden case to use capecitabine and cisplatin. (2)R1 operation(histologically positive PM, OM, LM, VM). (3)Infection or inflammatory case. (4)Severe heart disease. (5)Severe complicated case such as ileus, intestitial pneumonia, uncontrolled DM, liver cirrhosis etc. (6)Difficulty to join the trial due to psychosis nervous system damage. (7)Complicated other active cancer. (8)patient who want to be pregnant and/or pregnant woman. (9)Intend to make pregnant. (10)Active hepatitis type HB positive(HBs antigen, HBc antibody and HBs antibody). (11)Otherwise determined by investigators or site principal investigators to be unsuitable for participation in study).

研究者

发起方
SGCSG:Shimane Gstroenterological Vancer Study Group

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