跳至主要内容
临床试验/NL-OMON52652
NL-OMON52652招募中不适用

The relation between memory and exam performance - modulation with Methylphenidate - Memory and exam performance

niversiteit Maastricht0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
80

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

年龄范围
18 至 64(—)

入选标准

  • In the opinion of the investigator, the participant is capable of
  • understanding and complying with protocol requirements.
  • The participant has a body mass index of 18.5-30 kg/m2, inclusive, at the
  • medical screening.
  • The participant is aged 18 to 35 years, inclusive, at the time of informed
  • The volunteer is healthy, i.e. absence of all exclusion criteria and had
  • normal or corrected to normal static binocular acuity with or without
  • correction.
  • The participant signs and dates a written informed consent form before the
  • start of the experiment.
  • The participant has sufficient English language skills to read and understand
  • all instructions and perform the tasks in this study

排除标准

  • The volunteer has an uncontrolled, clinically significant neurologic,
  • cardiovascular, pulmonary, hepatic, renal, metabolic, gastrointestinal, or
  • endocrine disease or other ab-normality, which may impact the ability of the
  • subject to participate or potentially confound the study results.
  • The volunteer has existing major psychiatric symptoms.
  • The participant has known hypersensitivity to any component of the
  • formulation or methylphenidate or related compounds.
  • The participant has a history of drug abuse (defined as any illicit drug use)
  • or a history of alcohol abuse within 1 year prior to the first visit or is
  • unwilling to agree to abstain from alcohol from 24 hours prior to each test day
  • and/or drugs throughout the study.
  • The participant has been diagnosed with ADHD.
  • The participant has any sensory or motor deficits, which could reasonably be
  • expected to affect test performance.
  • Other exclusion criteria are excessive drinking (>20 glasses of
  • alcohol-containing beverages a week), pregnancy or lactation, use of medication
  • other than oral contraceptives, use of recreational drugs from 2 weeks before
  • until the end of the experiment, any condition in which gastrointestinal
  • motility might carry any risk.
  • The participant has dyslexia.

研究者

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