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
- Diseases
- Multiple sclerosis
- 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
Sites (28)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.