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Recruiting NCT05491031

MRI Biomarkers Predictive of Disability Progression in Patients With Multiple Sclerosis

No phase Interventional Multiple Sclerosis Magnetic Resonance Spectroscopy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: magnetic resonance spectroscopy.
Who it may be relevant to
Registry conditions: Multiple Sclerosis, Magnetic Resonance Spectroscopy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluation of MRI Biomarkers Predictive of Disability Progression in Patients With Multiple Sclerosis

Overview

The transition from relapsing-remitting multiple sclerosis to secondarily progressive multiple sclerosis (SPMS) is difficult to identify. Typically, SPMS is diagnosed retrospectively, with a significant delay, on the basis of a clinical history of progressive worsening, independent of relapses. Thus, SPMS is often associated with a considerable period of diagnostic uncertainty. The use of ultra-high field imaging can shed light on the mechanisms of disability progression thanks to its better spatial resolution and advanced imaging techniques. The new morphological imaging techniques make it possible to visualize chronic inflammatory lesions and to evaluate their evolution. It also allows for the precise measurement of brain atrophy, a reference in the evaluation of neurodegeneration. Metabolic imaging via proton spectroscopy allows the analysis of several promising cerebral metabolites that can provide information on cellular energy metabolism, mitochondrial function, or oxidative stress, and can help identify tissues at risk of neurodegeneration. Sodium imaging can provide information on axonal energy metabolism before the occurrence of stable and irreversible axonal damage. This technique is promising as an early marker of neurodegeneration.

Interventions

  • Other magnetic resonance spectroscopy
    Investigation of the association, in patients with multiple sclerosis, between MRI biomarker data at inclusion and progression of physical disability during follow-up (6, 12, 18 and 24 months) assessed by a composite endpoint EDSS plus (EDSS, 9HPT, T25FW)

Primary outcome measures

  • Identify imaging biomarkers at inclusion predictive of disability progression. [Time frame: up to 24 months]
Secondary outcome measures (3)
  • Determine the correlation between brain MRI and the concentration of imaging biomarkers (mmols) at 6, 12, 18 and 24 months. [Time frame: up to 24 months]
  • Develop realistic mathematical models of disease progression associated with clinical assessment of disability through dynamics, by the EDSS-plus score (EDSS scale from 0 to 10, T25FW in seconds, 9HPT in seconds). [Time frame: up to 24 months]
  • Develop an artificial intelligence algorithm to identify predictive markers for disability. The artificial intelligence algorithm utilizes patients' clinical (EDSSS-Plus Scale) and radiological (brain MRI) characteristics. [Time frame: up to 24 months]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years,
  • Duration of disease ≤ 25 years,
  • Irreversible disability ≤ 7 (permanent wheelchair use) on the EDSS scale

Exclusion criteria

  • Other progressive neurological disease,
  • Isolated radiologic syndrome (RIS),
  • Severe psychiatric pathology not in balance,
  • Change in dosage, discontinuation or initiation of a psychotropic treatment within the last month,
  • Change in background MS treatment for less than 3 months,
  • A course of corticosteroids (oral or intravenous) for less than one month,
  • Patient with a contraindication to MRI: pregnancy, metallic ocular foreign body (accidental splinters or others), pacemaker, implantable defibrillator, neurostimulator not compatible with MRI 7.0 T, cochlear implants and in general any electronic medical equipment implanted in an irremovable way: metallic cardiac valve, vascular clips (formerly implanted on cranial aneurysm), metallic prosthesis...),
  • Illiterate and non-French speaking patient: patient who is partially or completely unable to read and write French.
  • Patient benefiting from reinforced protection, i.e. minor, subject deprived of liberty by a judicial or administrative decision, subject staying in a health or social establishment, adult under legal protection and finally patient in emergency situation,
  • Pregnant or breastfeeding women, women of childbearing age who do not have effective contraception (hormonal/mechanical: per os, injectable, transcutaneous, implantable, intrauterine device, or surgical: tubal ligation, hysterectomy, total oophorectomy)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

France · 1 center
  • PoitiersUH — Poitiers

Identifiers

NCT: NCT05491031 · MR7T-PRADIMS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗