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临床试验/NCT00099229
NCT00099229已完成3 期

A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Tolerability of Licarbazepine 1000-2000mg/Day in the Treatment of Manic Episodes of Bipolar I Disorder Over 3 Weeks

Novartis Pharmaceuticals22 个研究点 分布在 3 个国家目标入组 320 人开始时间: 2004年11月1日最近更新:
适应症
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试验速览

阶段
3 期
状态
已完成
入组人数
320
试验地点
22
主要终点
Mean reduction in manic episodes and major depressive episodes from baseline to endpoint (Week 3).

研究概览

简要总结

This purpose of this study is to evaluate the safety and efficacy of Licarbazepine for the treatment of manic episodes of bipolar disorder.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Diagnosis of bipolar disorder (type I) with manic or mixed episodes (including patients with/without psychotic features or with/without a history of rapid cycling)
  • •In need of psychiatric treatment
  • •Cooperation and willingness to complete all aspects of the study

排除标准

  • •Current diagnosis other than bipolar I disorder
  • •History of schizophrenia or schizoaffective disorder
  • •Drug dependence within 1 month prior to study start or testing positive in a urine drug test
  • •Suicide attempt within 1 month prior to study start or at immediate risk of harm to self or others
  • •Any form of psychotherapy within 1 month prior to study start

结局指标

主要结局

Mean reduction in manic episodes and major depressive episodes from baseline to endpoint (Week 3).

次要结局

  • Major improvement in anxiety and depression from baseline to endpoint (Week 3)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (22)

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