Neuroimaging Changes in Hereditary Ataxia

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05160883
Collaborator
(none)
500
1
53.8
9.3

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Neuroimaging Changes in Hereditary Ataxia
    Actual Study Start Date :
    Jun 30, 2021
    Anticipated Primary Completion Date :
    Dec 25, 2025
    Anticipated Study Completion Date :
    Dec 25, 2025

    Outcome Measures

    Primary Outcome Measures

    1. neuroimaging information [from 2021 to 2025]

      neuroimaging information approached by MRI, including 3D-T1, T2, DTI, rsfMRI, SWI, ASL were collected

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • genetically diagnosed as Spinocerebellar ataxia
    Exclusion Criteria:
    • deny to follow-up

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Second Affiliated Hospital,Zhejiang University School of Medicine Hangzhou Zhejiang China 310009

    Sponsors and Collaborators

    • Second Affiliated Hospital, School of Medicine, Zhejiang University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Second Affiliated Hospital, School of Medicine, Zhejiang University
    ClinicalTrials.gov Identifier:
    NCT05160883
    Other Study ID Numbers:
    • Wulab-MRI in HA
    First Posted:
    Dec 16, 2021
    Last Update Posted:
    Dec 16, 2021
    Last Verified:
    Nov 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 16, 2021