About this trial
This project is to:
1. Quantify differences in axonal integrity and organization in aMS versus naPMS patients. 2. Quantify changes in axonal integrity and organization in aMS versus naPMS patients over a two-year period. 3. Validate the combination of imaging parameters that best differentiate aMS versus naPMS patients using histopathology.
Eligibility criteria
Qualifiers
active RRMS (n=100): Relapsing-remitting course and > 1 clinical relapse and/or signs of MRI activity (> 1 Gd enhancing lesion) during the last year before study enrollment.
non-active PMS (n=100): Progressive course (PPMS or SPMS) and no clinical relapses and/or signs of MRI activity during the last year before study enrollment.
Age 18-80 years old
No other neurological or psychiatric disorder
Disqualifiers
Pregnancy
Contraindication to MRI (eg, claustrophobia, metallic implants, pacemaker etc).
Inability to give consent
Trial design
Treatments tested in this trial
- MRI
- Neurocognitive examination for healthy subjects
- blood sampling
Treatment groups
Sponsors and collaborators
University Hospital, Basel, Switzerland
Lead sponsor
Swiss National Science Foundation
Collaborator