跳至主要内容
临床试验/JPRN-jRCT1080223122
JPRN-jRCT1080223122已完成Unknown

Drug use surveillance of Takecab tablets for Gastric ulcer, duodenal ulcer, and reflux esophagitis

Takeda Pharmaceutical Company Limited0 个研究点目标入组 3,183 人开始时间: 2016年3月1日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
3,183

研究概览

简要总结

In conclusion, from the results stated above, this surveillance raised no new concerns about the safety or efficacy of Takecab Tablets in participants with gastric ulcer, duodenal ulcer, or reflux esophagitis. Please refer to conclusions of "Adverse Events" and "Secondary Outcome Measures" sections for the details.

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • Participants with gastric ulcer, duodenal ulcer, and reflux esophagitis

排除标准

  • - Participants with previous history of hypersensitivity to ingredients in Takecab tablets
  • - Participants taking atazanavir sulfate or rilpivirine hydrochloride
  • - Participants meeting the criteria of scarring stage (S1, S2) of endoscopic classification defined by Sakita and Miwa at the start of the treatment with Takecab tablets, in the case that the target disease is gastric ulcer or duodenal ulcer
  • - Participants meeting the criteria of Grade N or Grade M of Los Angeles classification (Hoshihara's modification) at the start of the treatment with Takecab tablets, in the case that the target disease is reflux esophagitis.

研究者

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