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临床试验/CTRI/2017/03/007996
CTRI/2017/03/007996Other未知

Efficacy and safety of SPILs Rifaximin tablets, 200 mg Rifaximin in subjects with travelers diarrhea : A Randomized, Double blind, Parallel group, Active and Placebo Controlled, Clinical Endpoint Bio equivalence Study

Sun Pharmaceutical Industries Limited0 个研究点目标入组 1 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
Other
入组人数
1

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

入选标准

  • 1.Willing to participate and give written informed consent.
  • 2.Able and willing to comply with the protocol, including availability for all scheduled clinic visits.
  • 3.woman of child bearing potential - having a negative urine pregnancy test prior to beginning the therapy and ready to use effective contraceptive methods during the study.
  • 4.Experiencing at least three unformed stools recorded within the 24 hours

排除标准

  • 1.Pregnant, breast feeding or planning a pregnancy.
  • 2.Having active, uncontrolled, or clinically significant diseases
  • 3.Use of any drug such as aspirin or ibuprofen, which can cause GI bleeding

研究者

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