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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03356366
Other study ID # 2016-52
Secondary ID 2017-A00136-47
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 2, 2017
Est. completion date December 31, 2028

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

Multiple sclerosis (MS) is the first non-traumatic cause of disability in young people, responsible for physical but also cognitive deficits. MS is an inflammatory demyelinating and degenerative disease of the central nervous system. Recently, MRI technics have demonstrated their sensibility to the different processes involved in MS. Particularly, MRI has evidenced that the pathological process of MS is not restricted to the macroscopic lesions of the white matter but also involves the normal appearing white and grey matter. In the normal appearing brain tissue, demyelination, neuronal suffering and neuronal loss have been evidenced. Moreover, MRI has demonstrated the existence of brain functional reorganization processes that may limit the clinical expression of pathological injuries. Despite these important findings, the pathological underpinnings of irreversible disability are largely unknown. The present project aims to depict the main determinants of physical but also cognitive disability in patients with MS. To do this, a longitudinal study including 70 patients with MS using different MRI markers known to be sensitive to the different pathological aspects of MS will be performed. The relationships between these markers and the progression of disability will be assessed. Identification of the main pathological underpinnings of irreversible disability of MS will provide the most relevant therapeutic targets.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 70
Est. completion date December 31, 2028
Est. primary completion date January 16, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major patient, - Patient affiliated to a health insurance plan - Patient having signed free and informed consent after receiving detailed, understandable and honest information, - Patient with multiple sclerosis according to the criteria of Polman 2010 Exclusion Criteria: - Patients with the usual contraindications to MRI (pace-maker, agitation, metal splinters, claustrophobia etc.) - Patients at risk of non-compliance on examination: impaired understanding, confusion, involuntary movements, poor tolerance of prolonged supine - Patients with known allergy to gadolinium - Patients with renal insufficiency - Patients unable to give their consent: disorders of the comprehension, disturbances of vigilance, confusion ... - Pregnant and breastfeeding woman - Patients with a history of neurological or psychiatric pathology - Patients under guardianship or curatorship

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MRI 3T
Magnetic Resonance Imaging 3 Tesla
MRI 1,5T
Magnetic Resonance Imaging 1,5 Tesla
MRI 7T
Magnetic Resonance Imaging 7 Tesla

Locations

Country Name City State
France Assistance Publique - Hôpitaux de Marseille Marseille

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 Measurement of the Expanded Disability Status Scale (EDSS) value (score from 0 to 20) constituing the actual international reference scale to measure the level of disability caused by parkinson disease 5 years
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