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Validation of a Diagnostic Score for Encephalitis to Assess the Risk of Autoimmune Origin

Validation of a Diagnostic Score for Encephalitis to Assess the Risk of Autoimmune Origin

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05953974
Acronym
Val-Dia score
Enrollment
350
Registered
2023-07-20
Start date
2023-02-01
Completion date
2023-12-30
Last updated
2023-11-13

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

Conditions

Autoimmune Encephalitis, Autoimmune Encephalitis Caused by N-Methyl D-Aspartate Receptor Antibody (Disorder)

Keywords

Diagnostic score, auto-immune encephalitis

Brief summary

The investigators wish to test a diagnostic risk score for autoimmune encephalitis in case of encephalitis, previously validated by two American teams, in a retrospective analysis, according to the clinical and paraclinical data available in our database of the Reference Centre for Autoimmune Encephalitis and Paraneoplastic Neurological Syndromes of Professor Honnorat for patients with NMDAr, anti LGi1, anti CASPR2, anti GABAbr and anti GAD antibodies.

Interventions

OTHERClinical score of Granillo and al.

Compare the performance of the clinical prediction score of confirmed autoimmune encephalitis according to the type of antibody isolated from the CSF.

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

* Age \> 18 years old * Patient with a definite auto-immune encephalitis (Graus and al. 2016)

Exclusion criteria

* Uncomplete data in acute phase * Patient with several antibodies * Opposition

Design outcomes

Primary

MeasureTime frameDescription
Validation of a diagnostic score for encephalitis to assess the risk of autoimmune origin.At baselineComorbidities assessed by the Charlson score
Symptoms in the acute phaseAt baseline
Mode of onset of diseaseAt baseline
Results of lumbar punctureAt baseline
Results of antineuronal antibodies in CSFAt baseline
Results of antineuronal antibodies in serumAt baseline

Countries

France

Outcome results

None listed

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