NL-OMON46147已完成不适用
A Multicentre, Prospective, Longitudinal, Observational Natural History Study to Evaluate Disease Progression in Subjects with Usher Syndrome type 1B (USH1B) - Natural history of Usher syndrome type 1B
Oogziekenhuis Rotterdam0 个研究点目标入组 10 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
- 已完成
- 发起方
- 入组人数
- 10
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
- •Informed consent
- •Diagnosed with USH1
- •Molecular diagnosis of USH1B due to MYO7A mutations (homozygotes or compound heterozygotes)
- •Age >= 8 years
- •Visual acuity >= 20/640 in at least one eye
排除标准
- •Unable to communicate with suitable verbal/auditory and/or tactile sign language
- •Participation in clinical study with investigational drug in past 6 months
- •Pre-existing ocular conditions that would interfere with the interpretation of study
- •endpoints (e.g. glaucoma, corneal or significant lenticular opacities, cystoid macular oedema, macular hole) in both eyes
- •Complicating systemic diseases in which the disease itself, or the treatment for the disease,
- •can alter ocular function
- •Prior ocular surgery within 3 months
研究者
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