NCT02886611招募中不适用
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Genotype-phenotype Correlation
研究概览
简要总结
The study aims at searching for a genotype-phenotype correlation in patients with a genetic pathology of the ocular surface, in order to identify genetic abnormalities associated with the most severe clinical situations.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Cross Sectional
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •genetic pathology of ocular surface
排除标准
- •Agonal glaucoma
- •Low vision mostly related to retinal pathology
- •Pregnant or breast feeding patient
结局指标
主要结局
Genotype-phenotype Correlation
时间窗: baseline
次要结局
未报告次要终点
研究者
研究点 (1)
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