High-Tech MRI scans aim to unlock stroke recovery secrets
NCT ID NCT07339813
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 Hide 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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Ischemic stroke are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
RECRUITINGGif-sur-Yvette, Île-de-France Region, 91191, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a checklist and heart monitor stop repeat strokes?
- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next
- Zapping the spine while wearing a robotic ankle: a new way to help kids walk?
- Can a nurse and a neighbor help tame chronic disease?
- Can PET scans reveal hidden heart inflammation after a stroke?
- Two ways to catch a hidden heart rhythm after stroke