Fact CheckerSign in

NCT03981003Active, not recruiting

Serum Neurofilament-light Chain and GFAP Levels in Patients From the OFSEP Cohort at Different Landmarks of Multiple Sclerosis

Serum Neurofilament-light Chain and Glial Fibrillary Acidic Proten (GFAP) Levels in Patients From the OFSEP Cohort at Different Landmarks of Multiple Sclerosis

Source: ClinicalTrials.gov · Last updated 21 Oct 2026

Brief summary (registry, in English)

The investigators hypothesize that serum neurofilament-light chain (NfL) levels can provide information about the level of activity and progression of Multiple Sclerosis at different stages and landmarks of the disease. In addition, Glial Fibrillary Acidic Protein (GFAP) has also been identified as another serum biomarker of disability in MS.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1150 (estimated)
First submitted
23 May 2019
Start date
22 May 2019
Primary completion date
Jun 2027
Lead sponsor
Centre Hospitalier Universitaire de Nīmes
NCT number
NCT03981003

What you commit to

  • Study type: Observational
  • Planned participants: 1150
  • From 22 May 2019 to the primary completion date, Jun 2027
  • 28 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • The patient is in an exclusion period determined by a previous study.

Other illness

  • Clinically isolated syndrome (CIS) that does not meet the criteria of MS.
  • Radiologically isolated syndrome (RIS).
  • Patient with Neuromyelitis optica spectrum disorder.

Age

  • The patient is under 15 years old.

Other

  • Within the past three months, the patient has participated in another interventional study that may interfere with the results or conclusions of this study.
  • The patient is under judicial protection.
  • The patient refuses to sign the consent.
  • It is impossible to correctly inform the patient (inability to understand the study, language problem).
  • The patient is pregnant or breast-feeding.
  • Inability to answer questionnaires.

Who the study is looking for

  • The patient has been correctly informed.
  • The patient must have given their informed and signed consent.
  • The patient must be insured or beneficiary of a health insurance plan.
  • The patient is at least (≥)15 years old.
  • The patient has MS according to diagnosis criteria (Thompson et al. 2017) and:
    • Participates to the OFSEP-HD cohort (ancillary study);
    • Has a Expanded Disability Status Scale score comprised between 0 - 7.0;
    • With or without Disease Modifying Drug;
    • For Work Package 3: patients enrolled in any OFSEP-HD centre that meet landmark criteria for an active MS (relapse, or Expanded Disability Status Scale progression, or active MRI) during follow-up;
    • For Work Package 4: patients with a stable disease enrolled in OFSEP-HD study in Nîmes or Nantes University Hospitals.

Age in the registry: 15 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (28)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU D'amiens
Coordinator of this site? Confirm its status
AmiensFranceUnknown status
CHU de Besançon
Coordinator of this site? Confirm its status
BesançonFranceUnknown status
CHU de Bordeaux
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
CHU de CAEN
Coordinator of this site? Confirm its status
CaenFranceUnknown status
CHU de Clermont-Ferrand
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status
Hopital Henri Mondor
Coordinator of this site? Confirm its status
CréteilFranceUnknown status
CHU de DIJON
Coordinator of this site? Confirm its status
DijonFranceUnknown status
CHU de Grenoble
Coordinator of this site? Confirm its status
GrenobleFranceUnknown status
CHU de Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status
CHU de Limoges
Coordinator of this site? Confirm its status
LimogesFranceUnknown status
CHU de Lyon
Coordinator of this site? Confirm its status
LyonFranceUnknown status
Hôpital Timone
Coordinator of this site? Confirm its status
MarseilleFranceUnknown status
CHU de Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
CHU de Nancy
Coordinator of this site? Confirm its status
NancyFranceUnknown status
CHU de Nice
Coordinator of this site? Confirm its status
NiceFranceUnknown status
CHU de Nîmes
Coordinator of this site? Confirm its status
NîmesFranceUnknown status
Hopital Pitie-Salpetriere
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Fondation Rothschild
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Hôpital Saint-Antoine
Coordinator of this site? Confirm its status
ParisFranceUnknown status
CH de Poissy
Coordinator of this site? Confirm its status
PoissyFranceUnknown status
CHU de Potiers
Coordinator of this site? Confirm its status
PotiersFranceUnknown status
CHU de Rennes
Coordinator of this site? Confirm its status
RennesFranceUnknown status
CHU de Rouen
Coordinator of this site? Confirm its status
RouenFranceUnknown status
Chu de Saint Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceUnknown status
CHU de Strasbourg
Coordinator of this site? Confirm its status
StrasbourgFranceUnknown status
CHU de Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status
CHU de Tours
Coordinator of this site? Confirm its status
ToursFranceUnknown status
CHU de Martinique
Coordinator of this site? Confirm its status
Fort-de-FranceMartiniqueUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.