KCT0003061已完成未知
Study on the effects of mutations under inherited retinal disease in Korean
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
相似试验
招募中
1 期
Study on the correlation between gene mutation and TCM syndrome types in metastatic colorectal cancerMetastatic colorectal cancerITMCTR2100004411onghua Hospital Affiliated to Shanghai University of traditional Chinese Medicine
招募中
不适用
A study of the incidence of molecular mutations in newly diagnosed acute lymphoblastic leukemia (ALL) patients by Next-generation sequencing techniqueThai newly diagnosed ALL patients aged greater than 18 years.Acute lymphoblastic leukemia, Next-generation sequencing ,Molecular mutationsTCTR20240409003Siriraj Hospital Mahidol University140
招募中
Unknown
Effect of genetic polymorphism on antidiabetic medication in Indian patients with Type 2 DiabetesCTRI/2023/10/058414Chellaram Diabetes Research Centre
尚未招募
不适用
A study of incidence of molecular mutations in newly diagnosed acute myeloid leukemia (AML) patients by Next-generation sequencing techniqueewly diagnosed acute myeloid leukemia aged greater than 18 yearsAcute myeloid leukemia, molecular, incidence, next-generation sequencingTCTR20190227003The organization takes responsibility for initiating a study.139
未知
不适用
The investiaton of comprehenve genetic mutation in patients with HCC and hepatitis.HCC/hepatitisJPRN-UMIN000024590Chiba university50
