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Super MRI scans aim to unlock secrets of brain resilience

NCT ID NCT07202494

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study uses powerful MRI scanners to look at the brains and spinal cords of 700 people, including healthy volunteers and those with conditions like multiple sclerosis, Alzheimer's, and Parkinson's. The goal is to understand why some brains stay healthy while others decline. Researchers will track changes over two years to find better ways to diagnose and predict neurological diseases.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 700 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2025

Expected to finish

May 2030

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population includes 540 patients with various neurological diseases-multiple sclerosis (stratified by disability level), NMOSD/MOGAD, Alzheimer's disease, Parkinson's disease, ALS, epilepsy (temporal and non-temporal), and mild traumatic brain injury-and 160 healthy volunteers aged 18 to 90 years, evenly distributed by sex and age decade. All participants must provide informed consent, be free of major MRI contraindications, and have no uncontrolled somatic or psychiatric conditions. A subset of participants, including those with progressive conditions and healthy aging individuals, will undergo longitudinal follow-up at 1 and 2 years. The study aims to explore structural, functional, and metabolic brain changes across the lifespan and disease spectrum using ultra-high field MRI.

Ages

18 to 90 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age:Female or male, aged 18 years or older. * Health Status: No uncontrolled general diseases, such as cancer, autoimmune diseases, liver failure, severe or untreated high blood pressure, or severe rhythm disorders. No chronic psychiatric illnesses, including severe dementia. * MRI Compatibility: No contraindications for MRI exams (e.g., claustrophobia, metal foreign bodies, pacemakers, severe kidney failure). * Social Security Coverage: Participants must have social security coverage. * Informed Consent: The participant must have read, understood, and signed the informed consent after being adequately informed about the study. * Specific Disease Criteria (For Disease Groups): Specific inclusion criteria apply to each pathology, such as MS (based on McDonald criteria), NMOSD (Wingerchuk 2015), Alzheimer's (meeting NINCDS-ADRDA criteria), etc. Exclusion Criteria: * Pregnancy: Pregnant women are excluded from the study. * Inability to Provide Informed Consent: * Any participant who refuses to sign the informed consent or is unable to do so due to mental or physical conditions. * Refusal of MRI: Individuals who refuse to undergo brain MRI. * Contraindications for MRI:Participants with contraindications for MRI exams, such as claustrophobia, metal foreign bodies, pacemakers, or severe kidney failure. * Medical Conditions: Known allergy to Dotarem (contrast agent) for neuroinflammatory patients. Individuals with severe renal insufficiency or other conditions that prevent MRI scanning. Cognitive or Psychiatric Issues: Chronic psychiatric conditions, including severe dementia or cognitive dysfunction that could hinder participation. Legal or Institutional Restrictions: Adults under legal protection (e.g., under guardianship or curatorship). Individuals deprived of their liberty. Other Medical Conditions: Individuals with neurological diseases such as ischemic accidents, brain trauma, or encephalitis. Patients on treatments that would interfere with the study, as outlined for each disease. Allergy to Contrast Agent: Allergy to Dotarem for neuroinflammatory patients (MS, NMOSD, etc.). Inability to Adhere to Protocol: Participants who are unable or unwilling to comply with the study protocol.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Chu Timone

    RECRUITING

    Marseille, France

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