NCT02563418Unknown不适用
Feasibility of a Video-oculography in Patients With Huntington's Disease VOG-HD Study
University Hospital, Angers1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2014年5月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- saccadic measures with the eye tracker
研究概览
简要总结
The purpose of this study is to know the limits of feasibility of a reliable oculomotor record for patient with Huntington's disease.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
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
- •Corrected visual acuity >1/10
- •Aged over 18 years
- •Patient with the mutation that is to say the presence of an abnormal number of trinuclide: CAG> 38 in the first exon of the huntingtin gene.
- •Total Functional Capacity Scale (CFT) ≥ 3
排除标准
- •Patients or trustworthy person who have not given their written consent, informed and signed.
- •Patients are not affiliated or who are not entitled to Social Security
- •Private patients of liberty by administrative or judicial decision, or patients supervision
- •Associated disease with neurological repercussions
研究组 & 干预措施
Patient with Huntington's disease
Experimental
干预措施: Eye-tracking (Device)
结局指标
主要结局
saccadic measures with the eye tracker
时间窗: 1 day
one measure in the evening and one in the afternoon
次要结局
未报告次要终点
研究者
研究点 (1)
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