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临床试验/NCT01376271
NCT01376271已完成不适用

Special Drug Use Investigation for PAXIL (Paroxetine) Social Anxiety Disorder (Long-term)

GlaxoSmithKline0 个研究点目标入组 600 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
600
主要终点
The number of adverse events in Japanese subjects with social anxiety disorder treated with paroxetine tablets

研究概览

简要总结

The study is designed to evaluate the safety and efficacy of paroxetine on the long-term use in Japanese Social Anxiety Disorder (SAD) subjects.

研究设计

研究类型
Observational

入排标准

性别
All
接受健康志愿者

入选标准

  • Subjects who are diagnosed as having SAD
  • Subjects who are expected to use paroxetine tablets for the first time

排除标准

  • Subjects taking pimozide
  • Subjects taking monoamine oxidase (MAO) inhibitor or within two weeks after discontinuation of MAO inhibitor
  • Subjects with hypersensitivity to paroxetine

研究组 & 干预措施

Subjects prescribed paroxetine tablets

Subjects with SAD prescribed paroxetine tablets during study period

干预措施: Paroxetine (Drug)

结局指标

主要结局

The number of adverse events in Japanese subjects with social anxiety disorder treated with paroxetine tablets

时间窗: 1 year

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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