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Active, not recruiting Observational

Mechanisms of Disease Severity in Multiple Sclerosis: an Integrative Multimodal Study

NCT03369106 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2018-02-06
Last updated
2026-03-11

Condition(s) studied

Multiple Sclerosis

Investigational drug(s) / intervention(s)

Composite severity score calculation

Composite severity score calculation: Neurological examination, cognitive testing, and MRI exam

Study summary

This study will identify a combination of disease severity markers (genetic, immunology, epigenetic, imaging) associated with disease severity and progression in a cohort of patients with multiple sclerosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Clinically isolated syndrome or Multiple sclerosis (2010 Mc Donald criteria) * Sibling having Clinically isolated syndrome or Multiple sclerosis (2010 Mc Donald criteria) willing to participate to the study * Affiliated to the French social security or equivalent Exclusion Criteria: * Cyclophosphamide, mitoxantrone or methylprednisolone infusion within one month before inclusion * Multiple sclerosis relapse within one month before inclusion * Concomitant severe or uncontrolled disease

Primary outcome measure(s)

  • Change of Expanded Disability Status Scale (EDSS) — Baseline and 18 months
    Change in the Expanded Disability Status Scale (EDSS) which is the neurological assessment of disability related to multiple sclerosis. The EDSS measures disability status on a scale ranging from 0 to 10, with higher scores indicating more disability. Scoring is based on measures of impairment in eight functional systems on examination by a neurologist.

Trial sites (1)

FacilityCityRegionStatus
CIC Neurosciences Institut du Cerveau et de la Moelle Epinière Paris France
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 NCT03369106 on ClinicalTrials.gov ↗ ← All trials in France