NL-OMON34216招募中不适用
Cerebellar dysfunction and its compensation in presymptomatic carriers of dominant ataxia genes - Cerebellar changes in presymptomatic SCA-carriers
niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 50 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
- 招募中
- 发起方
- 入组人数
- 50
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
- 18 至 99（—）
入选标准
- •Proven mutation in one of the SCA genes
- •Age > 18 years
- •Free of ataxia
排除标准
- •Contraindications for MRI scanning (e.g. pacemaker)
- •Other neurological disorders
- •Gait disorder for any reason
研究者
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