Actively Recruiting
Study of the Visual Pathways Model for Understanding Neurodegeneration in Inflammatory and Demyelinating Central Nervous System Disorders
Led by University Hospital, Lille · Updated on 2025-08-20
100
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating neurodegenerative processes in neuroinflammatory diseases of the central nervous system such as multiple sclerosis, neuromyelitis optica spectrum disorders, and anti-MOG antibody-associated disorders. These conditions involve inflammation and damage to brain, optic nerve, and spinal cord tissues, affecting both white and grey matter. The study aims to better understand how these processes lead to clinical disability by using the visual pathways as a model to measure nerve loss and explore underlying mechanisms, including possible vascular involvement. The study involves patients experiencing an acute episode of optic neuritis who will be prospectively followed in a single group. Researchers will use various tools such as MRI sequences, optical coherence tomography angiography, pupillometry, and visual cognition evaluations to analyze neurodegeneration from structural and functional perspectives. Assessments will take place at inclusion, 1 month, 6 months, and 12 months to track changes over time. Participants will undergo detailed clinical exams, imaging scans, retinal and vascular assessments, and visual acuity tests throughout the study period. Researchers will measure outcomes including optic nerve sheath enhancement on MRI, retinal nerve layer atrophy, retinal microvascular changes, and brain lesion volumes. Safety and progression will be monitored with repeated evaluations up to 12 months after the acute event. The total study duration for participants is one year, focusing on understanding neurodegeneration in optic neuritis and related disorders.
CONDITIONS
Brief 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 has given written consent to participate
- Patient has 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 such as 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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At inclusion
Participants undergo clinical examinations including MRI sequences for research, pupillometry, OCT-angiography, and evaluation of visual cognition to assess optic neuritis and related neurodegenerative changes.
1 visit (in-person)
Duration - 12 months
Participants are followed up to monitor changes in optic nerve enhancement, retinal vascularization, brain lesions, and visual acuity over time.
Visits at 1 month, 6 months, and 12 months (in-person)
Trial Site Locations
Total: 1 location
1
Hop Fontan Chu
Lille, France, 59037
Actively Recruiting
Research Team
O
Olivier OUTTERYCK, MD
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
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here