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临床试验/NL-OMON53753
NL-OMON53753招募中不适用

Effects of transcranial ultrasonic stimulation on eye movements - Transcranial ultrasonic stimulation of the frontal eye fields

Radboud Universiteit Nijmegen0 个研究点目标入组 45 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
45

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

  • - Between 18-40 years of age
  • - Right handed
  • - The ability and agreement to provide informed consent, and the ability to
  • fulfil the study's requirements

排除标准

  • Under 18 years of age;
  • Current or planned pregnancy;
  • Claustrophobia;
  • A history or brain surgery or serious head trauma;
  • A history of or any close relatives (parents, siblings, children) with
  • epilepsy, convulsion, or seizure;
  • Predisposition for fainting spells (syncope);
  • A cardiac pacemaker or intra-cardiac lines;
  • An implanted neurostimulator;
  • Implanted medication infusion device;
  • Implanted metal devices or large ferromagnetic fragments in the head or upper
  • body (excluding dental wire), or jewellery/piercing that cannot be removed;
  • Use of a medical plaster that cannot or may not be taken off (e.g., nicotine
  • Cochlear implants;
  • Metal in the brain, skull, or elsewhere in your body (fragments, clips,
  • Diagnosed neurological or psychiatric disorders;
  • Use of psychoactive (prescription) medication (excluding anti-conception);
  • Skin disease at intended stimulation sites;
  • The consumption of more than four alcoholic units within 24 hours before
  • participation or any alcoholic units within 6 hours before participation day;
  • The consumption of recreational drugs within 48 hours before participation;
  • Calcifications in the brain.
  • All other criteria relevant to non-invasive brain stimulation as reported in
  • the Donders Standard Operating Procedures for Non-Invasive Brain Stimulation.

研究者

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