跳至主要内容
临床试验/NCT00358969
NCT00358969Unknown不适用

Guanfacine in the Treatment of Borderline Personality Disorder

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家开始时间: 2006年7月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
试验地点
1
主要终点
measures of impulsive aggression

研究概览

简要总结

This study is designed to investigate whether guanfacine (Tenex) is an effective treatment for borderline personality disorder (BPD), an illness often characterized by unstable mood and impulsive aggression. Guanfacine stimulates activity in the front portion of the brain, a region associated with attention and the control of behavior. We believe that guanfacine may improve symptoms of BPD by improving attention and aiding regulation of behavior.

详细描述

This is an 8-week treatment study designed to test whether guanfacine is an effective treatment for borderline personality disorder (BPD). Prior to taking the study medication, subjects will have medical and psychiatric evaluations, complete self-report questionnaires, do a functional MRI scan, and complete a set of cognitive tests. While taking the study medication, participants will meet weekly with a study doctor and be administered interviews and questionnaires. At the end of the 8-week trial, participants will be asked to repeat the MRI scan and cognitive tests.

研究设计

研究类型
Interventional
分配方式
Non 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 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • This study includes men and women between the ages of 18 and 55 who meet criteria for borderline personality disorder with impulsive aggression.

排除标准

  • Subjects must not currently be taking any psychiatric medications. Subjects must not meet criteria for current substance dependence, current major depression, bipolar disorder, or schizophrenia-spectrum disorders.

结局指标

主要结局

measures of impulsive aggression

measures of affective disturbance

measures of social and occupational functioning

measures of overall clinical status

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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