NCT01060800已完成不适用
The Genetics of Chiari Type I Malformation (CMI) With or Without Syringomyelia
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,000
- 试验地点
- 1
- 主要终点
- Genetic factors contributing to Chiari Type I malformation
研究概览
简要总结
Duke University Medical Center is investigating the hereditary basis of Chiari type I malformations with or without syringomyelia (CM1/S). Our research is aimed at learning if CM1/S is indeed caused by factors inherited through the family and, if so, which genes are involved.
研究设计
- 研究类型
- Observational
- 观察模型
- Family Based
- 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
- 未提供
排除标准
- 未提供
结局指标
主要结局
Genetic factors contributing to Chiari Type I malformation
时间窗: end of study
This study aims to identify genetic factors that contribute to or cause Chiari Type I malformation.
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
相似试验
已完成
不适用
Genetic Analysis of the Chiari I MalformationType I Arnold Chiari MalformationSyringomyeliaNCT00004738National Institute of Neurological Disorders and Stroke (NINDS)152
已完成
不适用
Identification of Genetic Mutations Involved in Chiari Type I MalformationsChiari Malformation, Type 1NCT05165030Assistance Publique - Hôpitaux de Paris40
进行中（未招募）
不适用
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical TrialsPrimary Ciliary DyskinesiaNCT06172374ReCode Therapeutics150
招募中
不适用
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2Charcot-Marie-Tooth Disease, Type Ia (Disorder)HMSNNCT01193088University of Iowa1,050
Enrolling By Invitation
不适用
Idiopathic Diseases of ManIdiopathic DiseaseRare DiseaseNCT01440218Scripps Translational Science Institute10