跳至主要内容
临床试验/ISRCTN52392534
ISRCTN52392534已完成未知

Efficacy of OROS-methylphenidate on specific executive functioning deficits in adults with Attention deficit hyperactivity disorder (ADHD)

Parnassia Bavo Academy (PBA) (Netherlands)0 个研究点目标入组 22 人开始时间: 2013年7月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
22

研究概览

简要总结

2014 results in https://www.ncbi.nlm.nih.gov/pubmed/24508533 (added 09/08/2019)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Between 18-55 years of age. The participants are of either sex. We included 22 adults with the combined subtype of ADHD, of which 17 were male and 5 were female.
  • 2. Diagnosis of ADHD, combined subtype

排除标准

  • 1. Having severe comorbid psychiatric disorders at time of the study screening (as measured by the Structured Clinical Interview for DSM disorders; SCID)
  • 2. Receiving treatment with stimulants, antipsychotics, clonidine, benzodiazepines, or beta-blockers <1 month before study participation
  • 3. Having any cognitive disorder like dementia or amnesic disorder
  • 4. Mental retardation
  • 5. Being pregnant or nursing

研究者

发起方
Parnassia Bavo Academy (PBA) (Netherlands)

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