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临床试验/EUCTR2004-000202-49-EE
EUCTR2004-000202-49-EE进行中(未招募)不适用

Efficacy of Aripiprazole in Combination with Valproate or Lithium in the Treatment of Mania in Patients with Bipolar I Disorder Partially Nonresponsive to Valproate or Lithium Monotherapy Revised Protocol Number 03, incorporating Amendments 2, 3 and 5+ Pharmacogenetics Blood Sample Amendment 1

Bristol-Myers Squibb International Corporation0 个研究点目标入组 575 人开始时间: 2005年2月22日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
575

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Patients with Bipolar I Disorder, manic or mixed episode, with or without psychotic features, as defined by DSM-IV-TR and confirmed by the M.I.N.I. who are partially nonresponsive to lithium or valproate monotherapy;
  • - Patients who have a history of at least one previous manic or mixed episode of sufficient severity to require hospitalization, and/or treatment with a mood stabilizer or antipsychotic agent;
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients presenting clinically with a current DSM-IV -TR diagnosis of :delirium, dementia, amnesia, amnestic or other cognitive disorders, or a psychotic disorder(e.g. schizoprenia or schizoaffective disorder). Also patients with borderline, paranoid, histronis, schizotypal, schzoid or antisocial personality disorder.

研究者

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