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Clinical Trials in France / NCT05056740
Recruiting Observational

Combined Analysis of Inflammatory Biomarkers for CNS Autoimmune Diseases Diagnostic

NCT05056740 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2020-06-01
Last updated
2026-06-26

Condition(s) studied

Central Nervous System Diseases

Investigational drug(s) / intervention(s)

Data analysis

Data analysis: Analysis of the data from routine care at the end of the diagnostic work-up

Study summary

Project rationale:

Since 2017, multiple sclerosis diagnosis should match the new McDonald criteria in which a "no better explanation than MS" should be fulfilled. However, many patients present with red flags that lead to a complex diagnostic work-up. There are no available biomarkers that permit to confirm or roll out MS diagnosis in such cases. Therefore, we lack biological markers that can help in the diagnosis of patients presenting with suspected MS.

Many studies have found that serum and cerebrospinal fluid (CSF) cytokines could help to differentiate MS from other diseases such as neuromyelitis optica spectrum disorders (i.e., IL-6) or neurosarcoidosis (i.e., sIL-2R). Serum and CSF kappa free light chains have also shown good diagnosis performance in MS. In daily practice, our MS tertiary center already perform the analysis of CSF concentrations of IL-1β, sIL-2R, IL-6, IL-10, and serum and CSF kappa and lambda free light chains to roll out other central nervous system (CNS) autoimmune diseases in patients presenting with white matter hyperintensities (WMH).

Objective:

To correlate CSF IL-1β, sIL-2R, IL-6, IL-10, serum and CSF kappa and lambda free light chains with the final diagnosis in patients presenting to our MS tertiary center with suspected MS to identify a specific inflammatory biomarker profil involved in MS and other CNS autoimmune diseases.

The methodology:

This is an observational study. All patients ongoing a routine diagnostic work-up for suspected MS from june 2020 to june 2022 in our MS tertiary center will be analyzed. Cerebrospinal fluid IL-1β, sIL-2R, IL-6, IL-10, serum and CSF kappa and lambda free light chains will be correlated with the final diagnosis to ultimately find MS associated biomarkers.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients referred to our center for the diagnostic work-up of White Matter Lesions * Patients that need a routine blood analysis * Patients that need a routine CSF analysis * Non opposition to research consent Exclusion Criteria: * Patients with a contraindication to perform spinal tap (increase bleeding risk medicine or disease) * Patients with a contraindication to MRI (metal prosthesis…)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier Universitaire de Nice Nice France Recruiting

More Centre Hospitalier Universitaire de Nice trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05056740 on ClinicalTrials.gov ↗ ← All trials in France