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Clinical-immunological Features of DNER Ataxia

Conditions
DNER Ataxia
Registration Number
NCT05225896
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

Using a retrospective cohort of 34 patients with DNER ataxia, we will characterize clinical presentation, tumor associations, and outcomes.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
34
Inclusion Criteria
  • Patient > 18 years old
  • Patient with neurological disorder
  • Patient with DNER antibodies in sera or CSF
Exclusion Criteria
    • No available clinical data
  • Patient without DNER antibodies or neurological disorder

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Modified Rankin scale (mRS)6 month after the beginning of study

Residual neurological disability as assessed by the modified Rankin scale (mRS) score at last visit)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

HCL Hôpital Neurologique / Groupement EST

🇫🇷

Bron, France

HCL Hôpital Neurologique / Groupement EST
🇫🇷Bron, France

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