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临床试验/JPRN-UMIN000011625
JPRN-UMIN000011625已完成1 期

Phase I/II study of biweekly docetaxel, cisplatin, and S-1 combination neoadjuvant chemotherapy in patients with stage III gastric cancer - Phase I/II study of biweekly docetaxel, cisplatin, and S-1 combination neoadjuvant chemotherapy in patients with stage III gastric cancer

Yokohama City University Medical Center0 个研究点目标入组 51 人开始时间: 2013年9月2日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
51

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. with active double cancer within 5 years except intramucosal cancer 2. with a history of severe allergy 3. with active infectious disease(over 38 degrees C) 4. Women in pregnancy, at risk of pregnancy, or hoping to become pregnant. 5. Men who want their partners to become pregnant 6. with a history of cardiac infarction in recent 6 months 7. with a continuous administration of steroids 8. patient who needs continuous administration of Flucytosine, fenitoin or walfarin karium 9. with ulceration on digestive tract and/or bleeding from the ulcer 10. with uncontrollable diarrhea or watery stool 11. with active hepatitis B Ag and/or hepatitis C Ab 12. with serious complication as followings, -Interstitial pneumonia -Pulmonary fibrosis -paralysis on bowel -ischemic heart diseases 13. Any patients judged by the investigator to be unfit to participate in the study

研究者

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