Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia

Hereditary Ataxia Clinical Trial

Official title:
Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia

Status Recruiting

Clinical Trial Summary

The investigators aimed to find appropriate biomarkers such as serum neurofilament light chain in reflecting disease severity in hereditary ataxia from a large cohort during long-term follow-up. The disease severity is indicated by clinical scales and brain MRI tests.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05160870
Study type	Observational
Source	Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact	Yi Dong
Phone	+ 8618367129345
Email	dongyi720@zju.edu.cn
Status	Recruiting
Phase
Start date	June 30, 2021
Completion date	December 25, 2025

View Details

See also
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Active, not recruiting	`NCT06152133` - Telerehabilitation, Core Stability Exercises and Hereditary Ataxia (TRCore-ataxia)	N/A
Recruiting	`NCT05160883` - Neuroimaging Changes in Hereditary Ataxia
Completed	`NCT00202397` - Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia	Phase 2
Recruiting	`NCT01360164` - Safety and Efficacy of Umbilical Cord Mesenchymal Stem Cell Therapy for Patients With Hereditary Ataxia	Phase 1/Phase 2