EUCTR2006-004073-10-DE进行中（未招募）不适用
Effect of Atomoxetine and a standardized behavior therapy on attention deficits in adult ADHD - Atomoxetine and adult ADHD
niversity of Giessen0 个研究点开始时间: 2006年8月16日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •Actual diagnosis of ADHD according to DSM IV
- •Age 18 to 50
- •Both sexes
- •Declaration of informed consent for all clinical measures
- •Normal IQ (Estimated by a short IQ test during the screening)
- •Normal ECG findings
- •Sufficient knowledge of the German language to follow instructions and training procedure
- •In- and out-patients
- •Consent to a highly effective birth control method (failure rate less than 1%) for female patients in childbearing years
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •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
- •Other psychiatric disorder according to DSM IV
- •Any neurological disorder
- •Tachykardia, hyperpiesia or very low blood pressure
- •Liver malfunctions
- •Contraindication for the usage of Atomoxetine as listed in the companies safety information
- •Intake of antibiotics, azol-antimycotics, antihistamines or antiarrhythmics
- •History of allergic reaction to Atomoxetine
- •Female patients who are pregnant or nursing
- •Other medication that affects the central nervous system
- •Paticipation in other clinical trials
研究者
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