Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT05487989

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hop Fontan Chu

Lille, France, 59037

Actively Recruiting

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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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