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临床试验/NCT00222482
NCT00222482已完成不适用

A Double-Blind and Placebo Controlled Assessment of Depakote ER in Borderline Personality Disorder

University of Minnesota0 个研究点目标入组 15 人开始时间: 2003年3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
15
主要终点
Symptom Checklist 90

研究概览

简要总结

This study examines the effect of Depakote ER versus placebo in a randomized trial of borderline personality disorder. Patients all participate in DBT therapy and those who are not responsive are assigned to either Depakote ER or placebo for up to 12 weeks. Borderline Personality Symtoms are measured and side-effects are assessed.

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
21 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients with the diagnosis of borderline personality disorder between the ages of 21 adn 55 years old. Must be in good physical health -

排除标准

  • Major psychiatric illness on Axis I - schizophrenia or bipolar disorder. May not have current MDD. May not be dependent on illicit substances or alcohol.

结局指标

主要结局

Symptom Checklist 90

次要结局

  • Barratt Impulsivity Scale

研究者

申办方类型
Other

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