NCT03959605已完成不适用
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 48
- 试验地点
- 1
- 主要终点
- Number of genetics variants
研究概览
简要总结
Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •children with albinism
- •father and mother of children with albinism
排除标准
- •sign of albinism except fovea plana in father or mother of children with albinism
- •ophthalmological abnormalities making access to the fundus with OCT impossible
结局指标
主要结局
Number of genetics variants
时间窗: 1 month
among the genes involved in albinism, identification of those presents in parents of children with albinism
次要结局
未报告次要终点
研究者
研究点 (1)
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