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NCT04918225: MAP-MS
Motor Asymmetry in Progressive Multiple Sclerosis Patients
trial testing Magnetic Resonance Imaging in Multiple Sclerosis, Primary Progressive in 46 participants. Completed in 10 February 2026.
10 February 2026
Quick facts
| Lead sponsor | Rennes University Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 46 |
| Start date | 3 November 2021 |
| Primary completion | 10 February 2026 |
| Estimated completion | 10 February 2026 |
| Sites | 1 location across France |
Drugs / interventions tested
- Magnetic Resonance Imaging
- Neurological examination
- Multiple Sclerosis Functional Composite
- Physiotherapist examination
Conditions studied
- Multiple Sclerosis, Primary Progressive — all drugs for Multiple Sclerosis, Primary Progressive →
- Multiple Sclerosis, Secondary Progressive — all drugs for Multiple Sclerosis, Secondary Progressive →
Sponsor
Rennes University Hospital
Who can join
Adults 18 to 60, any sex, with Multiple Sclerosis, Primary Progressive or Multiple Sclerosis, Secondary Progressive. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Project Rational A better understanding of the causes of physical disability is an important unmet need in progressive Multiple Sclerosis patients. Progressive Multiple Sclerosis patients most often present a worsening pyramidal syndrome of lower and, to a lesser extent, upper limbs (Lublin et al., 2014) suggesting a strong corticospinal tract involvement. The systematic high resolution Magnetic Resonance Imaging exploration of lesions location and severity, as well as extra-lesional tissue, on pan-medullar and encephalic motor tracts offers the opportunity to better understand the pathological mechanism associated with motor impairment. Scientific aims This project will follow a twofold approach. First, the investigators will consider an "inter-patient" approach where independent and absolute Magnetic Resonance metrics for each limb will be related to disability. Second, the investigators will consider an "intra-patient" approach (i.e. comparing differences of Magnetic Resonance metric and of clinical score from the left and the right side in the same patient). For this purpose, progressive Multiple Sclerosis patients with asymmetric motor impairment will be studied. Confronting clinical and Magnetic Resonance Imaging metric value asymmetries indeed offers the unique opportunity to free oneself from many confounding factors such as genetics, age, duration of disease evolution, acquisition bias, etc. These two approaches will allow us to precisely study the impact of local factors such as Multiple Sclerosis lesions located on motor tracts on motor disability. Methodology The investigators propose an observational multicenter cross-sectional and prognostic study. This study will involve two French centers (Rennes, Marseille) and will include a total of 40 progressive Multiple Sclerosis patients with an asymmetrical motor deficit. Twenty sex and age matched controls will be needed to calibrate quantitative Magnetic Resonance imaging (magnetization transfer ratio). Encephalic and pan medullar structural and quantitative Magnetic Resonance images will be acquired at inclusion and clinical follow-up examinations will be performed at inclusion and 24 months. Detailed motor evaluation "per limb" will be performed, including the motor American Society Injury. Association sub-score and upper and lower limbs muscle strength measurements using a dynamometer.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
LesionSCynth: A simple parametric lesion synthesis method to improve spinal cord lesion segmentation in low-data scenarios.
Walsh R, Kaur P, Karimi D, Kerbrat A, et al · · 2025 · PMID 41322363 · DOI 10.1162/imag.a.1029
Verify or expand the search:
- PubMed search for NCT04918225
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04918225 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Rennes University Hospital
- Last refreshed: 19 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04918225.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing