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Clinical Monitoring, MRI and Neuro-Ophthalmology of a Cohort of Patients With a Clinically Isolated Syndrome (CIS) (cinocis)

U

University Hospital, Lille

Status

Completed

Conditions

Multiple Sclerosis
Clinically Isolated Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT03541226
2012_56
2013-A00475-40 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to develop tools to detect, measure, monitor and predict axonal damage in the course of CIS and during Multiple sclerosis (MS), in order to be able to consider as early as possible an adaptation of the background treatment in patients with MS. patients with radiological criteria of poor long-term clinical course.

Enrollment

134 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any patient who has had a CIS of less than 4 months (+/- 15 days), with at least 1 inflammatory lesion on his initial brain MRI or with normal brain MRI associated with the presence of oligoclonal bands in the CSF,

Exclusion criteria

  • Atypical CIS for a first relapse of multiple sclerosis (extensive myelitis, bilateral retrobulbar optic neuritis immediately)
  • CIS dating more than 4 months (+/- 15 days)
  • Corticotherapy in the last 4 weeks

Trial contacts and locations

1

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Central trial contact

Patrick Vermersch, MD,PhD; Olivier Outteryck, MD,PhD

Data sourced from clinicaltrials.gov

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