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High-Tech MRI scans aim to unlock stroke recovery secrets

NCT ID NCT07339813

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 3T and 7T MRI scanners to create detailed maps of brain activity and connections in 100 stroke patients and 10 healthy volunteers. The goal is to understand how the brain reorganizes after a stroke and to identify patterns linked to motor deficits. Findings may guide future rehabilitation and brain-computer interfaces.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help create better rehabilitation strategies and improve brain-computer interfaces for stroke patients.
What could go wrong
This is an observational study, not a treatment trial. It may not directly lead to new therapies, and results depend on complex data analysis.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 110 people

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

Started

Dec 2025

Expected to finish

Jan 2029

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

18 to 70 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: Patients * 1-MRI-confirmed diagnosis of a first ischemic stroke occurring more than 6 months prior to inclusion. * 2-Persistent upper-limb motor deficit resulting from the stroke. * 3-Absence of significant cognitive impairment: MMSE score ≥ 27 assessed as part of clinical care. * 4-Age between 18 and 70 years. * 5-Validation by the inclusion validation committee. * 6-Signed informed consent after clear and fair information about the study. Healthy volunteers: * 1-Age between 18 and 70 years. * 2-No history of neurological or psychiatric disease. * 3-Signed informed consent after clear and fair information about the study. Exclusion Criteria: Patients: * 1-Recurrent stroke. * 2-Severe aphasia or severe speech disorders preventing adequate interaction for the protocol. * 3-Severe auditory or visual impairment. * 4-Disorders of comprehension, attention, or neglect affecting understanding of study motor tasks. * 5-Associated conditions with an estimated life expectancy of less than 2 years. * 6-History of brain surgery, craniectomy, or cranioplasty. * 7-Other causes of motor disability. * 8-Alcohol consumption the day before or on the day of the examination, or use of illicit psychotropic substances within 48 hours prior to MRI. * 9-Absolute contraindications to MRI, including pregnancy; intracorporeal metallic foreign bodies; pacemakers; non-MRI-compatible neurostimulators; cochlear implants; implanted medical devices (electronic or non-electronic) implanted for less than 6 weeks; metallic heart valves; stents, coils, carotid or neurosurgical clips; implantable ports; infusion pumps; non-removable piercings; tattoos or permanent makeup larger than 5 cm on the head, neck, trunk, or upper limbs; transdermal devices with metallic components; intrauterine devices (except Mirena); dental appliances larger than 4 cm; or health conditions incompatible with MRI comfort and safety (e.g., acute respiratory or cardiac failure, inability to remain supine, bedridden state, claustrophobia). * 10-Individuals not covered by a social security system. * 11-Individuals under enhanced protection, including pregnant or breastfeeding women, persons deprived of liberty, legally protected adults, or patients in emergency situations. * 12-Pregnant or breastfeeding women, or women of childbearing potential refusing a pregnancy test. Healthy volunteer: * 1-Absolute contraindications to MRI as listed above. * 2-Individuals not covered by a social security system. * 3-Individuals under enhanced protection, including pregnant or breastfeeding women, persons deprived of liberty, legally protected adults, or patients in emergency situations.

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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

  • NeuroSpin, CEA

    RECRUITING

    Gif-sur-Yvette, Île-de-France Region, 91191, France

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Other studies related to the condition(s) this trial covers.