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Clinical-immunological Features of DNER Ataxia

Clinical-immunological Features of DNER Ataxia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05225896
Acronym
CLIMDA
Enrollment
34
Registered
2022-02-07
Start date
2021-06-15
Completion date
2022-06-30
Last updated
2022-02-07

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

Conditions

DNER Ataxia

Keywords

DNER antibodies, autoimmune cerebellar ataxia, Hodgkin lymphoma

Brief summary

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

Interventions

GENETICDescription of clinical characteristic and genetic tumors

This is a non-interventional study involving clinical data and biological samples (DNA). Clinical data are collected for the center and samples are already stored in biobank repositories and collected as part of good clinical practice in the diagnostic process of patients with suspected autoimmune encephalitis, meaning that the standard diagnostic and therapeutic approaches will not be altered in the selected study population. Patients have already gave explicit written consent for biological specimens sampling and storage at the Centre de Ressources Biologiques des Hospices Civils de Lyon (CRB-HCL) (including tissue, cells or biological fluids) and genetic analysis for research purposes. Additionally, patients will be informed about the present study.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Modified Rankin scale (mRS)6 month after the beginning of studyResidual neurological disability as assessed by the modified Rankin scale (mRS) score at last visit)

Countries

France

Contacts

Primary ContactBastien JOUBERT, MD
bastien.joubert@chu-lyon.fr04.27.85.54.60
Backup ContactMarine VILLARD, RCA
marine.villard@chu-lyon.fr04.27.85.54.60

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026