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临床试验/NL-OMON50997
NL-OMON50997招募中不适用

Objectifying the day-time response variation of (lis)dexamphetamine in adults with ADHD. - day-time response variation of (lis)dexamphetamine

Academisch Medisch Centrum0 个研究点目标入组 16 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
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Participant is aged between 18 * 60 years at time of diagnosis
  • Participant is diagnosed with ADHD according to the DSM 5 criteria
  • Participant started pharmacotherapy treatment with dex or lisdex but no real
  • preference for the type of amphetamine exists according to the practitioner
  • Participant is able to provide written informed consent
  • Participant is able and willing to comply with the study protocol

排除标准

  • No diagnosis for ADHD
  • Currently other psychopharmacotherapy treatment than dex or lisdex
  • Currently other psychopharmacotherapy parallel to dex or lisdex

研究者

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