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临床试验/JPRN-UMIN000002703
JPRN-UMIN000002703已完成未知

Alleviating Effect of Lafutidine on Toxicity of S-1: Adjuvant Chemotherapy of Gastric Cancer (AEOLUS) - Alleviating Effect of Lafutidine on Toxicity of S-1: Adjuvant Chemotherapy of Gastric Cancer (AEOLUS)

Pharma Valley Center , Shizuoka Industrial Foundation0 个研究点目标入组 200 人开始时间: 2009年11月3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
200

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) Patient with active double cancer (synchronous double cancer and metachronous double cancer), excluding carcinoma in situ (lesions equal to intraepithelial or intramucosal cancer) judged to have been cured with local treatment. 2) Patient with administration contraindication of S-1 and Lafutidine 3) Patient with regular use of H2-blocker, PPI, furucytocin, fenytoin, or warfarin. 4) Patients with the past history of severe allergic reactions. 5) Patient with severe complications, such as paralytic ileus, bowel obstruction, interstitial pneumonitis, pulmonary fibrosis, or uncontrollable diabetes mellitus, arrhythmias, heart failure, liver cirrhosis, and active hepatitis) 6) Severe watery diarrhea. 7) pregnant or nursing patient or with intent to bear baby 8) Exclude the patients who are recognized as inadequate patients by doctors with responsibility in this trial.

研究者

发起方
Pharma Valley Center , Shizuoka Industrial Foundation

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