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临床试验/JPRN-UMIN000021006
JPRN-UMIN000021006已完成未知

Comparative study between Tokisyakuyakusan and mecobalamin for the efficacy in patients with olfactory dysfunction post-respiratory infection. - Comparative study between Tokisyakuyakusan and mecobalamin for the efficacy in patients with olfactory dysfunction post-respiratory infection.

Kanazawa Medical University0 个研究点目标入组 100 人开始时间: 2016年2月13日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
100

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 60years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients who have rhinosinusitis which is subjected to effect on olfactory dysfunction post-respiratory infection. 2) Patients who used Tokisyakuyakusan or mecobalamin within the last two weeks (It will be eligible if they do not use those medicine for at least two weeks). 3) Patients who are pregnant, suspected to be pregnant or breastfeeding. 4) Patients who desire to bear children 5) Patients who are considered not to be eligible by the investigator.

研究者

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