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Clinical Trial Summary

The purpose of the study is to detect the presence of autoantibodies and autoantigens in cerebrospinal fluid early (<48 hours) following spinal cord trauma.

The study also aims to define the central or peripheral origin of autoantibodies by looking for their simultaneous presence at the blood level and to evaluate the prognostic value of the presence of autoantibodies within the cerebrospinal fluid, as well as on the initial clinical severity than on the recovery potential.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03249129
Study type Observational
Source University Hospital, Lille
Contact
Status Withdrawn
Phase
Start date September 2018
Completion date April 2021

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