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临床试验/JPRN-UMIN000014707
JPRN-UMIN000014707已完成2 期

Efficacy and safety of neoadjuvant chemotherapy by S-1 plus cisplatin for Stage III esophageal squamous cell carcinoma: A phase II trial - Neoadjuvant chemotherapy by S-1 plus cisplatin for esophageal squamous cell carcinoma

agoya University Hospital0 个研究点目标入组 30 人开始时间: 2014年7月30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
30

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 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Synchronous or metachronous (within 5 years) malignancies other than carcinoma in situ 2) Uncontrolled infection 3) Pregnant women, possibly pregnant women, wishing to become pregnant, and nursing mothers 4) Psychiatric disease 5) Continuous systemic steroid therapy 6) Uncontrolled severe complications (DM, hypertension, diarrhea, et al.) 7) Patient with symptomatic cardiovascular disease or asymptomatic disease but have been treated 8) Symptomatic CNS metastasis 9) Interstitial lung disease or pulmonary fibrosis 10) Hypersensitivity for S-1 or cisplatin 11) Flucytosine, phenytoin, warfarin potassium or aminoglycoside antibiotic administration 12) Intestinal bleeding 13) Judged by physician inadequate for inclusion in this trial

研究者

发起方
agoya University Hospital

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