Neuroimaging Changes in Hereditary Ataxia

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05160883

Enrollment

500

Registered

2021-12-16

Start date

2021-06-30

Completion date

2025-12-25

Last updated

2021-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hereditary Ataxia

Brief summary

This study aim to investigate the neuroimaging changes of hereditary ataxia patients, especially in the SCA3 patients in preclinical or mild stage.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Inclusion criteria

* genetically diagnosed as Spinocerebellar ataxia

Exclusion criteria

* deny to follow-up

Design outcomes

Primary

Measure	Time frame	Description
neuroimaging information	from 2021 to 2025	neuroimaging information approached by MRI, including 3D-T1, T2, DTI, rsfMRI, SWI, ASL were collected

Countries

China

Outcome results