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临床试验/JPRN-UMIN000004787
JPRN-UMIN000004787已完成2 期

Phase II study for evaluation of volume reduction surgery for Stage IV advanced gastric cancer effectively treated with S-1 based combination chemotherapy - PerSeUS-GC01

PerSeUS-GC0 个研究点目标入组 40 人开始时间: 2010年12月24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
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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)History of severe hypersensitivity (allergy) to any medicines 2)Administration contraindication of S-1 and combination agent 3)Continuous use of flucytosine, phenytoin or warfarin potassium 4)Active infection 5)Severe complications, such as intestinal paralysis, ileus, interstitial pneumonitis or pulmonary fibrosis, uncontrolled diabetes mellitus, heart failure, renal failure and hepatic failure 6)Watery stools or diarrhea 7)Massive pleural or abdominal effusion 8)Active double cancer 9)Pregnant or nursing females. 10)Males who are planning partners' pregnancy. 11)Not suitable for participation with any other reasons

研究者

发起方
PerSeUS-GC

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