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临床试验/NL-OMON45518
NL-OMON45518招募中不适用

An observational neuroimaging and neurophysiological study investigating the visual pathway in Huntington*s disease. - Visual pathway in HD.

eids Universitair Medisch Centrum0 个研究点目标入组 60 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
60

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 64(—)

入选标准

  • * Between 18 and 65 years of age at time of visit
  • * Ability to undergo MRI scanning
  • * Written informed consent must be obtained from the participant;If the participant is a manifest HD gene carrier:
  • * Gene positive tested with CAG repeat length of * 36 in the HTT gene
  • * UHDRS-TMS > 5;If the participant is a premanifest HD gene carrier:
  • * Gene positive tested with CAG repeat length of * 36 in the HTT gene
  • * UHDRS-TMS * 5;If the participant is a control subject:
  • * Gene negative tested for HD or without family history of HD
  • * No other known cognitive, neurological or psychiatric disorders

排除标准

  • * Impaired primary visual ability (<0.5) or ophthalmic disorders
  • (including amblyopia or color vision deficiency)
  • * Additional major co-morbidities not related to HD
  • (e.g. cardiovascular diseases, hypertension, diabetes mellitus, and/or other neurological disorders)
  • * History of severe head injury
  • * Contra-indication for MRI (metallic implants/devices, claustrophobia)
  • * Participation in intervention trials
  • * Pregnancy
  • * Inability to understand the information about the protocol

研究者

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