Motor Asymmetry in Progressive Multiple Sclerosis Patients
Launched by RENNES UNIVERSITY HOSPITAL · Jun 2, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the causes of motor difficulties in patients with progressive forms of Multiple Sclerosis (MS), specifically focusing on those who have uneven strength or movement in their limbs. Researchers aim to better understand how brain and spinal cord damage affects physical abilities by using advanced imaging techniques, like MRI scans, to look closely at the areas of the brain and spinal cord that control movement. The study will involve 40 patients with progressive MS who show noticeable differences in strength between their limbs, as well as 20 healthy individuals for comparison.
To be eligible, participants must be between 18 and 60 years old and have been diagnosed with either Primary or Secondary Progressive MS. They should have a specific level of disability and not have experienced any significant symptoms for at least three years. During the study, participants will undergo MRI scans and detailed assessments of their muscle strength over a period of 24 months. This research could help improve our understanding of MS and ultimately lead to better treatments for those affected by the disease.
Gender
ALL
Eligibility criteria
- 1. - Inclusion Criteria:
- 1.1/ Patients:
- • Aged between 18 and 60 years.
- • Primary Progressive Multiple Sclerosis or Secondary Progressive Multiple Sclerosis as defined by Mac Donald revised criteria in 2017.
- • Expanded Disability Status Scale lower or equal to 8.0, at inclusion.
- • asymmetric motor deficit. The motor deficit asymmetry will be defined by a difference of 3 or more at the American Society Injury. Association motor sub-score per limb between the right lower limb and the left lower limb.
- • No evidence of focal inflammatory activity for at least 3 years (no clinical relapse, no gadolinium enhancement on an Magnetic Resonance Imaging scan and no new T2 lesion)
- • Provided written informed consent according to the Institutional review board approval
- • Affiliated to the French healthcare system.
- 1.2 / Controls:
- • Aged between 18 and 60 years, sex and age matched with patients.
- • Provided written informed consent according to the Institutional review board approval
- • Affiliated to the French healthcare system.
- 2. - Non-inclusion criteria:
- 2.1 /Patients:
- • cerebellar Expanded Disability Status Scale sub score higher than pyramidal Expanded Disability Status Scale sub score.
- • Relapse or corticosteroids in the 30 days preceding inclusion.
- • Other neurological diseases.
- • Lack of ability to understand the Institutional review board consent form.
- • Magnetic Resonance contraindications.
- • Pregnancy and breastfeeding.
- • Major persons subject to legal protection (legal safeguards, guardianship,curatorship), persons deprived of their liberty
- 2.2 / Controls:
- • Personal history of central nervous related disease
- • Familial history of Multiple Sclerosis.
- • Personal history of spinal cord injury.
- • Personal history of spondylotic myelopathy.
- • Magnetic Resonance Imaging contraindication.
- • Lack of ability to understand the Institutional review board form.
- • Major persons subject to legal protection (legal safeguards, guardianship, curatorship), persons deprived of their liberty
- • Pregnancy and breastfeeding.
About Rennes University Hospital
Rennes University Hospital, a leading academic medical center in France, is dedicated to advancing healthcare through innovative clinical research and trials. With a strong emphasis on patient-centered care, the hospital integrates cutting-edge scientific research with clinical practice, fostering collaboration among multidisciplinary teams. Its commitment to excellence is reflected in its robust infrastructure and expertise in various medical fields, enabling the development and evaluation of novel therapies and treatment protocols. By participating in clinical trials, Rennes University Hospital aims to enhance patient outcomes and contribute to the global body of medical knowledge.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rennes, , France
Marseille, , France
Patients applied
Trial Officials
Anne Kerbrat, MD
Principal Investigator
CHU Rennes
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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