Actively Recruiting

Age: 18Years - 65Years
All Genders
ID05487989

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

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 has given written consent to participate
  • Patient has 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 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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

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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

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