跳至主要内容
临床试验/JPRN-UMIN000010687
JPRN-UMIN000010687已完成未知

A clnical study to assess inhibitory effect of bepotastine besilate OD tablet to compare with fexofenadine hydrochloride and pseudoephedrine hydrochloride combination tablet in patients with cedar pollinosis in the OHIO Chamber. - A clnical study to assess inhibitory effect of bepotastine besilate OD tablet to compare with fexofenadine hydrochloride and pseudoephedrine hydrochloride combination tablet in patients with cedar pollinosis in the OHIO Chamber.

Samoncho Clinic0 个研究点目标入组 56 人开始时间: 2013年5月25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
56

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 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with mucosal lesion of the nose and eyes. 2)Patients with severe or requiring treatment needed Allergic Rhinitis. 3)Patients who received steroid injections within 6 months. 4)Patients with respiratory disease such as asthma. 5)Patients with past history of anaphylaxis. 6)Patients who have anaphylaxis with these drugs. 7)Patients with pregnancy, delivery or lactation.

研究者

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