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临床试验/JPRN-UMIN000026441
JPRN-UMIN000026441已完成未知

Comparative test on the occurrence rate of side effects accompanying duloxetine oral dosing timing - Study on the incidence of adverse reactions due to internal timing of duloxetine

Saku Central Hospital0 个研究点目标入组 60 人开始时间: 2017年4月15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
60

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
26years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1 Patients under 25 years of age 2 A patient with suicide ideas and suicide attempts in the past 3 Patients with a history of hypersensitivity to the ingredients of this drug 4 Patients during monoamine oxidase inhibitor administration or within 2 weeks after discontinuation of administration 5 Patients with high liver damage or advanced renal impairment 6 Patient with poor control of closed angle glaucoma

研究者

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