Trials / Unknown
UnknownNCT05160870
Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 500 (estimated)
- Sponsor
- Second Affiliated Hospital, School of Medicine, Zhejiang University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
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
Timeline
- Start date
- 2021-06-30
- Primary completion
- 2022-12-25
- Completion
- 2025-12-25
- First posted
- 2021-12-16
- Last updated
- 2022-01-12
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05160870. Inclusion in this directory is not an endorsement.