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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03659981
Other study ID # 2018-01
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 20, 2018
Est. completion date May 18, 2024

Study information

Verified date July 2023
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study is an opportunity to assess grey matter damage at the earliest phase of Multiple Sclerosis (MS) allowing to a better understanding of its origins and its impact and disease severity. This study is a preliminary longitudinal study to precisely depict the kinetic of grey matter damage and the links with disease aggravation. Thirty MS patients without time and spatial dissemination criteria (only one symptomatic MRI lesion detected) but with oligoclonal bands detected on cerebro spinal fluid analysis will be included for a monocentric transversal MRI study at 7T to assess grey matter injury. Clinical and neuropsychological assessments will be performed in the population the same day of a multi-parametric MRI. A longitudinal clinical and MRI follow up will be performed during 2 years.


Description:

The present study is an opportunity to assess grey matter damage at the earliest phase of MS allowing to a better understanding of its origins and its impact and disease severity. This study is a preliminary longitudinal study to precisely depict the kinetic of grey matter damage and the links with disease aggravation. Thirty MS patients without time and spatial dissemination criteria (only one symptomatic MRI lesion detected) but with oligoclonal bands detected on cerebro spinal fluid analysis will be included for a monocentric transversal MRI study at 7T to assess grey matter injury. Clinical and neuropsychological assessments will be performed in the population the same day of a multi-parametric MRI. A longitudinal clinical and MRI follow up will be performed during 2 years.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 32
Est. completion date May 18, 2024
Est. primary completion date May 19, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - First presumed inflammatory demyelinating event in the central nervous system involving either the optic nerve, the spinal cord, a brain hemisphere, or the brainstem without spatial and time dissemination criteria - Oligoclonal bands on CSF analysis - Age between 18 and 45 - No previous history of neurological symptoms suggestive of demyelination - No steroids in the month before MRI - First MRI within six months after the first clinical episode Exclusion Criteria: - Possible alternative diagnoses - Previous history of neurological or psychiatric disease - Previous administration of immunosuppressive drugs - Pregnancy - Patient unable to give his consent for the study or patient under tutorship

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MRI 7T
The imaging parameters will come from the 7 Tesla Siemens MRI

Locations

Country Name City State
France Assistance Publique Des Hopitaux de Marseille Marseille Paca

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of cortical lesions Cortical lesion detection on 7T MRI at baseline 2 hours
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