Actively Recruiting
VIsual Pathways Model in Neuro-inflammatory Disorders
Led by University Hospital, Lille · Updated on 2025-08-20
100
Participants Needed
1
Research Sites
287 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In neuroinflammatory diseases of the central nervous system (CNS) such as multiple sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD) and anti-MOG antibody-associated disorders (MOGAD), neuronal degeneration is the consequence of inflammatory and demyelinating lesions in the brain, optic nerve and spinal cord. Both white and grey matter are systematically affected. Lesions of the perivascular spaces containing cerebrospinal fluid (CSF) and meningeal inflammation seem to play an important role in the pathophysiology of these neuroinflammatory diseases. Currently, the interrelation of all these aspects is not clearly established in the pathophysiology of these diseases. In order to better understand the mechanisms that lead to and underlie the clinical disability of patients with these diseases, we need in vivo study models that allow the in-depth study of the neurodegenerative process and the identification of its causes. In this perspective, we make the hypothesis that the visual pathways model is very relevant to measure neuro-axonal loss and to explore the different mechanisms involved in neurodegeneration during MS and other CNS demyelinating diseases. Researchers have at their disposal many tools that allow them to analyse and quantify the neurodegenerative process in a reproducible and very precise manner from a structural and functional point of view, while taking into account possible vascular involvement (MRI, optical coherence tomography - angiography, etc…).
CONDITIONS
Official Title
VIsual Pathways Model in Neuro-inflammatory Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female
- Aged between 18 and 65 years
- Presenting a clinical picture of optic neuritis for less than 4 weeks, confirmed by neuro-ophthalmological assessment
- Patient having given written consent to participate in the study
- Patient with social insurance
- Patient willing to comply with all study procedures and duration
You will not qualify if you...
- History of optic neuritis on the same side as the recent episode
- History of retinal pathology such as retinal detachment, glaucoma, retinopathies, or retinal surgery
- Diabetes
- Chronic alcohol intoxication
- Contraindications to MRI
- Pregnant women
- Persons under protective supervision (e.g., guardianship)
- Minors
- Persons deprived of their liberty
- Administrative reasons including inability to receive informed information, inability to participate in the entire study, lack of social security coverage, or refusal to sign consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hop Fontan Chu
Lille, France, 59037
Actively Recruiting
Research Team
O
Olivier OUTTERYCK, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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