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临床试验/KCT0003061
KCT0003061已完成未知

Study on the effects of mutations under inherited retinal disease in Korean

Yonsei University0 个研究点目标入组 560 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
560

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
4(Month) 至 75(Year)(—)
性别
All

入选标准

  • •1) Inherited retinal disease
  • •2) Age between 4 months and 75 years
  • •3) Subject who has clinically confirmed visual impairment including night blindness or photophobia. Subject should meet one of the following criteria
  • •- pigmentary retinopathy in both eyes
  • •- reduced response in photopic or scotopic electroretinogram in both eyes
  • •- photoreceptor degeneration in optical coherence tomography in both eyes

排除标准

  • •1) unilateral retinal disease
  • •2) Subject who had previously confirmed genetic testing
  • •3) Age less than 4 months or more than 75 years
  • •4) When congenital infection or trauma are suspicious for the cause of retinal disease
  • •5) When age-related macular degeneration, myopic degeneration, autoimmune origin are suspicious for the cause of retinal disease
  • •6) No visual impairment or normal electroretinogram (e.g., benign fleck)
  • •7) Illiterate subject who can not understand informed consent
  • •8) Foreigners

研究者

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