NL-OMON46590招募中不适用
Rate of progression in USH2A related retinal degeneration - RUSH2A
Jaeb Center For Health Research0 个研究点目标入组 25 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
- 发起方
- 入组人数
- 25
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
- 2 至 99（—）
入选标准
- •2.2.1 Study Participant Inclusion Criteria
- •1. Willing and able to complete the informed consent process
- •2. Ability to return for all study visits over 48 months if in the natural history study
- •3. Age * 8 years
- •4. At least 2 pathogenic or likely pathogenic mutations in USH2A gene from a clinically certified lab report
排除标准
- •2.2.2 Study Participant Exclusion Criteria
- •1. Mutations in genes that cause autosomal dominant RP, X-linked RP, or presence of biallelic mutations in autosomal recessive RP/retinal dystrophy genes other than USH2A
- •2. Expected to enter experimental treatment trial at any time during this study
- •3. History of more than 1 year of cumulative treatment, at any time, with an agent associated with pigmentary retinopathy (including hydroxychloroquine, chloroquine, thioridazine, and deferoxamine)
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