Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia
NCT05160870 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500
Last updated 2022-01-12
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.
Conditions
- Hereditary Ataxia
Sponsors & Collaborators
-
Second Affiliated Hospital, School of Medicine, Zhejiang University
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-06-30
- Primary Completion
- 2022-12-25
- Completion
- 2025-12-25
Countries
- China
Study Locations
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