EUCTR2008-004425-42-NL进行中（未招募）不适用
eurocognitive testing in children with ADHD
适应症
相关药物
试验速览
- 阶段
- 不适用
- 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
- •Written informed consent from parents having parental responsibility or from the legal guardian. In the case of a child aged 12 years the written informed consent of the child is needed in addition to that of parents having responsibility/legal guardian;
- •Aged 8-12 years;
- •Able to communicate with the investigator in Dutch;
- •Confirmed DSM IV diagnosis of ADHD (Based on examination by a psychiatrist or pediatrician);
- •Classifying as clinical ADHD on the AVL(ADHD Vragenlijst”);
- •Currently receiving treatment with (immediate or sustained release) methylphenidate
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •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
- •Use of drugs other than methylphenidate with known psychotropic effects.
研究者
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