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临床试验/NCT00029614
NCT00029614已完成2 期

Psychopharmacology of Adolescents With AUD and ADHD

University of Pittsburgh2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2006年5月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
24
试验地点
2
主要终点
decrease in ADHD symptoms

研究概览

简要总结

The purpose of this study is to compare the effectiveness and safety of atomoxetine in the treatment of adolescents with coexisting alcohol or substance use disorders and Attention Deficit Hyperactivity Disorder (ADHD).

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
None

入排标准

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

入选标准

  • Adolescents, ages 13-18
  • Meets criteria for alcohol and/or substance use disorder and attention deficit hyperactivity disorder.

排除标准

  • Adolescents who are pregnant.
  • Have a history of seizure disorder, other neurological or medical disorder for which medication treatment may present a considerable risk.
  • History of pervasive development disorder, schizophrenia or other psychotic disorders, organic mental disorders or eating disorders.
  • Currently on other psychotropic medications from which discontinuation would present a significant risk.
  • A current episode of major depressive disorder or a diagnosis of bipolar disorder.
  • Diagnosis of dependence for any substance other than marijuana.
  • Adolescents with a full-scale IQ below 80.

结局指标

主要结局

decrease in ADHD symptoms

decrease in the quantity and frequency of alcohol and other substance use

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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