跳至主要内容
临床试验/CTRI/2011/08/001981
CTRI/2011/08/001981已完成4 期

To compare the efficacy and tolerability of methylphenidate and atomoxetine in children with attention deficit hyperactivity disorder.

Department of Psychiatry0 个研究点目标入组 69 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
69

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients from 6 to 15 years of age with the diagnosis of Attention Deficit Hyperactivity Disorder according to Diagnostic and Statistical Manual of Mental Disorders-IV-Text Revision.
  • Patients with moderate to severe illness as assessed by Clinical Global Impressions Severity Scale.
  • Patients whose parents are willing to provide informed consent for participating in the study.

排除标准

  • Patients with history of non-response or adverse drug reactions to methylphenidate or atomoxetine in the past.
  • Patients who have taken any medication for ADHD in past one month.
  • Patients with history of heart disease, seizures, bipolar affective disorder, psychotic illness, pervasive developmental disorder, substance abuse, anxiety, mental retardation or tic disorder.

研究者

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