NL-OMON50300尚未招募不适用
Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1F (RUSH1F) - RUSH1F
JAEB Center for Health Research0 个研究点目标入组 2 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
- 尚未招募
- 发起方
- 入组人数
- 2
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational non invasive
入排标准
- 年龄范围
- 2 至 64（—）
入选标准
- •1. Willing and be able to complete the informed consent process, by patient
- •self of parents in case of minors
- •2. Ability to return for all study visits over 48 months if in the natural
- •history study
- •3. Age 8 years and older
- •4. Have retinal dystrophy caused by mutations in the PCDH15 gene, as identified
- •by a clinically certified lab
排除标准
- •1. Have other mutations in your DNA that could cause retinal degeneration
- •2. be planning to enter a study, testing treatments for retinal degeneration
- •during the time of this study
- •3. have a history of treatment that could have affected the retina
- •4. Have had certain eye surgeries that may affect the tests for this study
研究者
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