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临床试验/NCT00216723
NCT00216723已完成不适用

Efficacy and Safety of Aripiprazole in Patients With Schizophrenia or Bipolar Disorder

Korea Otsuka Pharmaceutical Co., Ltd.2 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2004年4月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
3,000
试验地点
2

研究概览

简要总结

This is a multicenter,open-label,prospective study of Aripiprazole use in patients with schizophrenia and bipolar disorder.

详细描述

This is a multicenter,open-label,prospective study of Aripiprazole use in patients with schizophrenia and bipolar disorder.

Qualified schizophrenia patients will be enrolled to an 12-week treatment phase of Aripiprazole by physician's assessment.

Qualified bipolar disorder patients will be enrolled to an 8-week treatment phase of Aripiprazole by physician's assessment.

This study will be continued for 6 years. The final report of Aripiprazole PMS will be submitted to KFDA on December 28, 2009.

研究设计

研究类型
Observational
观察模型
Ecologic Or Community
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with a schizophrenia or schizoaffective disorder or bipolar disorder according to DSM-IV criteria
  • Age: more than 18 years of age

排除标准

  • Unqualified patients judged by study investigator(s)

研究者

申办方类型
Industry

研究点 (2)

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