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Artificial Intelligence-Assisted Magnetic Resonance Imaging for Quality, Efficiency and Equity in the National Health Service (NHS) Care of Multiple Sclerosis

Sponsor: Queen Mary University of London

NCT ID: NCT07111637

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
AI software (device)
How long the study runs
Study runs about 22 months (dates as stated)
About the drug or intervention
AI software — device: icobrain ms is an Artificial Intelligence (AI)-assistive software which quantifies brain Magnetic Resonance Imaging (MRIs) and summarises clinically relevant findings for patients with Multiple Sclerosis in structured electronic radiological reports and annotated images.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 99 Years
Who
All
Number of participants
1,336
Started
2025-06-14
Last checked
2026-08

Plain English Summary

What is this study?

  • • Testing a new treatment for multiple sclerosis
  • • NA - 1,336 participants
  • • Multiple Sclerosis (MS) is a long-term disease that affects over 150,000 people in the UK

Who can take part?

  • • Ages 18 Years to 99 Years
  • • Diagnosed with multiple sclerosis

Where?

  • • London - Barts Health NHS Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Multiple Sclerosis (MS) is a long-term disease that affects over 150,000 people in the UK. Starting treatment early is important for managing Multiple Sclerosis (MS). It is also essential to monitor the treatment to see if it is working and to switch treatments if needed. Magnetic resonance imaging (MRI) is the only accepted tool to monitor how well the treatment is working. Current evaluation of brain Magnetic resonance imaging (MRI) scans requires visual inspection, of which sensitivity is degraded by human, and technical factors, such as lack of time, fatigue of radiologists, and lack of standardization of image acquisition protocols across the National Health Service (NHS). MRI-readings can be significantly enhanced by artificial intelligence (AI)-assistive software. Evidence suggests the rate of new lesion detection to be 3 - 4 times higher when using assistive software compared to visual inspection of MRI scans. In this study, an Artificial Intelligence (AI) software called "icobrain ms." developed by the company "icometrix" (Leuven, Belgium) is tested. This tool helps track MS by measuring changes in the brain using MRI scans. The AI can highlight problem areas and create reports that doctors can use to make better decisions about participants' treatment. The aim of the study is to prove that icobrain ms can be used to assist the neuro-radiologist with their visual assessment of MRI scans by a radiologist, and that it will help clinicians make more informed decisions about participants' current MS treatment.

Multiple Sclerosis

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 99 Years
  • Who can join: All genders

What the study is looking for

  • ✓Clinically Isolated Syndrome suggestive of demyelination (CIS) or definitive diagnosis of MS.
  • ✓Undergoing MRI head investigation.
  • ✓On an MS DMT pathway.
  • ✓Access to a smartphone, tablet or computer.

Who cannot take part

  • ✗patients with Multiples Sclerosis participating in a randomly assigned controlled CTIMP (participating in a single arm...
See the full criteria
Inclusion Criteria: * Clinically Isolated Syndrome suggestive of demyelination (CIS) or definitive diagnosis of MS. * Undergoing MRI head investigation. * On an MS DMT pathway. * Access to a smartphone, tablet or computer. Exclusion Criteria: * patients with Multiples Sclerosis participating in a randomised controlled CTIMP (participating in a single arm study may be included, provided this is in line with the other protocol).

Where Is This Study? (1 UK site)

Barts Health NHS Trust

London E1 4NS, United Kingdom

Recruiting
Site contact (verified)
Thomas Dr CampionPrincipal Investigator
Data sourced from ClinicalTrials.gov · Last verified: 2026-08