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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05645185
Other study ID # 820
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2021
Est. completion date October 1, 2022

Study information

Verified date December 2022
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Paraneoplastic neurological syndromes (PNS) are rare complications of cancer occurring in 0.01% of cases. Their clinical, biological and radiological presentation is heterogeneous and may constitute a diagnostic challenge. Anti-Ma2 PNS are rare diseases with a guarded prognosis. They are most often associated with a seminoma-like testicular tumor but can also be associated with lung cancer. Classically, they present as limbic, diencephalic and/or brainstem encephalitis. Anti-Ma2 antibodies target intracellular receptors and are characteristic of a particular form of encephalitis. Atypical manifestations including narcolepsy-cataplexy, weight gain, sexual dysfunction and motor neuron syndrome have been described and explain the difficulty in diagnosing anti-Ma2 associated PNS. It seems interesting to better characterize the phenotypes of Ma2 patients in order to optimize the diagnosis and follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date October 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Neurological disorder - Anti-Ma2 positivity in sera or CSF - Patient > 18 years old Exclusion Criteria: - Patient without clinical data - Patient without Ma2 antibody in sera or CSF

Study Design


Intervention

Diagnostic Test:
Diagnosis test
Tests can be used: immunofluorescence, immunodot, western blot, tests CBA on sera or CSF.

Locations

Country Name City State
France Centre de référence des syndromes neurologiques paranéoplasiques et encéphalites autoimmunes Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rankin score Follow up and survival (rankin score) 12 month after diagnosis
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