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临床试验/JPRN-jRCT1080222951
JPRN-jRCT1080222951未知Unknown

Drug use surveillance of Takecab tablets Supplement to Helicobacter pylori eradication

TAKEDA PHARMACEUTICAL COMPANY LTD.0 个研究点目标入组 500 人开始时间: 2015年8月31日最近更新:
适应症

试验速览

阶段
Unknown
发起方
入组人数
500

研究概览

简要总结

暂无简介。

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 who meet the following criteria will be included.
  • 1.Participants receiving H. pylori eradication treatment for the first time
  • 2.Participants for whom H. pylori eradication with Takecab tablets or proton pump inhibitor + amoxicillin + clarithromycin was found unsuccessful and who will receive eradication treatment with amoxicillin and metronidazole

排除标准

  • Participants who meet any of the following criteria will not be included. Refer to the Contraindications and Precautions section of the package insert of antimicrobials used in triple therapy.
  • 1.Participants with previous history of hypersensitivity to ingredients in Takecab tablets
  • 2.Participants taking atazanavir sulfate or rilpivirine hydrochloride

研究者

发起方
TAKEDA PHARMACEUTICAL COMPANY LTD.

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