Optic Neuritis Clinical Trial
— DTI et NOIOfficial title:
Can Diffusion Tensor Imaging (DTI) of the Optic Ways Contributes to Predict the 6 Months Prognosis of Optic Neuritis (ON)?
Verified date | November 2022 |
Source | Rennes University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Can diffusion tensor imaging (DTI) of the optic ways contributes to predict the 6 months prognosis of Optic Neuritis (ON)?
Status | Completed |
Enrollment | 40 |
Est. completion date | June 24, 2022 |
Est. primary completion date | June 24, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - Age from 18 to 55 years old - Clinically suspected optic neuritis defined as a sudden decrease of the visual acuity and/or a damage to the field of vision and/or a defect of the colour vision and/or retro-orbital pain with a relative afferent pupillary defect (except if the optic neuropathy is bilateral or symmetrical), in the absence of a severe retinal macular pathology, and in the absence of a toxic or iatrogenic intake (ethambutol, vfend) - Clinical optic neuritis duration < 15 days - First episode of an inflammatory ON - No corticosteroids in the month before - Indication to a corticosteroid therapy at high dose to cure the felt symptomatology - Retinal nerve fibre layer (RNFL) thickness upper 75 µm at initial stage - Isolated ON, multiple sclerosis or NMO (Neuro Myelitis Optica) - SD (Spectrum Disorder) context - Having signed informed consent for participating in the study Exclusion Criteria: - Contra-indication to MRI - Cardiac pacemaker or defibrillator implant - Neurosurgical clips - Cochlear implants - Intra-orbital or encephalic foreign bodies - Stents implanted since less than 4 weeks and osteosynthesis equipment implanted since less than 6 weeks - Claustrophobia - Persons subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty - Eye examination suggests a pre-existing eye abnormality that could affect the visual function (amblyopia, strong myopia…) - Pregnant or breastfeeding women |
Country | Name | City | State |
---|---|---|---|
France | CHU de Rennes | Rennes |
Lead Sponsor | Collaborator |
---|---|
Rennes University Hospital |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Study of DTI markers in the assessment of the visual prognosis at 6 months of an inflammatory NO based on RNFL thickness (< ou > 75 µm) | MRI | Month 6 | |
Secondary | Study of DTI markers in the assessment of the visual prognosis at 6 months of an inflammatory NO based on visual acuity and/or sensible damage to the field of vision | MRI | Month 6 | |
Secondary | Comparison of the structural anomalies detected in DTI to the standard morphological MRI (Coronal T2 Fat-Sat MRI and T1 Gadolinium) for ON | MRI | Month 6 |
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