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Recruiting NCT04010214

A Registered Cohort Study on Cerebellar Ataxia in the Organization in South-East China for Cerebellar Ataxia Research (OSCCAR)

— Observational Cerebellar Ataxia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention.
Who it may be relevant to
Registry conditions: Cerebellar Ataxia. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Registered Cohort Study on Cerebellar Ataxia

Overview

Cerebellar ataxia is a form of ataxia originating in the cerebellum. Cerebellar ataxia can occur as a result of many diseases and may present with symptoms of an inability to coordinate balance, gait, extremity and eye movements. To understand the clinical and genetic characteristics of cerebellar ataxia, we establish a registered cohort to follow up Chinese patients with cerebellar ataxia.

Interventions

  • Other No intervention
    No intervention

Primary outcome measures

  • The incidence of hereditary cerebellar ataxia [Time frame: Up to 20years]

Eligibility criteria

Inclusion criteria

  • Patients with cerebellar ataxia based on the diagnoses of tow neurologists
  • Relatives of patients with cerebellar ataxia
  • Unrelated healthy controls
  • Participants or legal guardian(s) willing and able to complete the informed consent process

Exclusion criteria

  • Participants are unable to comply with trial procedures and visit schedule

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Department of Neurology ,First Affiliated Hospital Fujian Medical University — Fuzhou

Identifiers

NCT: NCT04010214 · MRCTA,ECFAH of FMU[2019]195

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗