JPRN-UMIN000047382招募中未知
Patient registry of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) - HOPE-net
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 100
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
- ot applicable 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Patients considered unsuitable for participation in the study by the investigator.
研究者
相似试验
已完成
不适用
Genotype/Phenotype Correlation of Movement Disorders and Other Neurological DiseasesMovement DisordersMyoclonusNervous System DiseasesTic DisordersTremorNCT00001667National Institute of Neurological Disorders and Stroke (NINDS)300
尚未招募
不适用
development patient data set by recording and maintenance a registry at the national levelCTRI/2019/06/019661Indian Council of Medical Research
已完成
不适用
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular DiseasesCharcot-Marie-Tooth DiseaseMuscular DystrophySpinal Muscular Atrophy With Respiratory Distress 1Amyotrophic Lateral SclerosisNeuromuscular DiseasePeroneal Muscular AtrophySpinal Muscular AtrophyMotor Neuron DiseaseNCT02532244Nemours Children's Clinic230
招募中
不适用
Biomarker Research in Inherited Movement DisordersInherited Movement DisordersSpinocerebellar AtaxiasHyperkinetic DisordersNCT05034172Assistance Publique - Hôpitaux de Paris4,000
招募中
不适用
VIsual Cerebral ConnecTivity On Functional Magnetic Resonance Imaging in Patients With Hereditary REtinal DystrophiesVision Functional Brain Networks in Patients With Hereditary Retinal DystrophiesNCT04648124Fondation Ophtalmologique Adolphe de Rothschild200