EUCTR2017-000739-15-Outside-EU/EEA进行中（未招募）1 期
A Double-Blind Placebo Controlled Study of Atomoxetine Hydrochloride for the Treatment of ADHD in Children and Adolescents With ADHD and Comorbid Dyslexia
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •patients must meet Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV) criteria for Attention-Deficit/Hyperactivity Disorder (ADHD)
- •patients must achieve a score of 80 or more on the Full Scale Intelligence Quotient
- •child or adolescent patients must be 10 to 16 years old
- •must be able to communicate in English
- •must be able to swallow capsules
- •be reliable to keep appointments for clinic visits and all related tests
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 209
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •patients who weigh less than 25 Kg or greater than 70 Kg
- •patients with a history of alcohol or drug abuse on a repeated basis within the past 3 months
- •patients with documented history of autism, Asperger's syndrome or pervasive developmental disorder
- •females who are pregnant or breastfeeding
- •patients with a history of severe allergy to more than one class of medications
- •patients with documented history of bipolar I or bipolar II disorder, or psychosis
研究者
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