Validation and implementation of advanced MRI protocols
Official title: Validation and Implementation of 3T MRI Research Protocols
Run by Institut National de la Santé Et de la Recherche Médicale, France · NCT04866940 · Data updated 2026-11-12
This study is testing new MRI techniques to see if they can improve brain imaging for both healthy people and patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 230 (estimated) |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France Government |
| Locations | 1 site (Toulouse) |
| Status | Recruiting |
| Started | May 12, 2021 |
| Main results expected | May 12, 2027 |
| Study ends | May 12, 2027 |
| Registry record updated | February 18, 2026 |
| Trial ID | NCT04866940 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include healthy individuals and patients aged 18 and older who can remain still during the MRI procedure.
✕Probably not a fit
Patients with psychiatric disorders, cognitive impairments, or contraindications to MRI will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research focuses on optimizing MRI acquisition sequences using a dedicated 3T MRI imager located at the INSERM premises. The study involves healthy participants and patients, where various sequences will be tested to enhance image quality for brain studies. Each sequence will be evaluated by a neuroradiologist and a research engineer to determine optimal parameters for future tests. The goal is to ensure that the imaging techniques remain at the forefront of research applications in neuroscience.
Why it matters
Potential benefit: If successful, this study could lead to improved MRI imaging techniques that enhance the diagnosis and understanding of brain pathologies.
How similar studies have gone: Other studies have shown success in optimizing MRI protocols, indicating that this approach is both relevant and potentially beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female, 18 years of age or older * Ability to cooperate and remain motionless for up to 1 hour (and lying down for 1.5 hours) * Ability to understand the instructions given * Subject who has given written and informed consent prior to any examination required by the research) * Subject affiliated to a social security system or benefiting from an equivalent system Exclusion Criteria: * Persons deprived of liberty by judicial or administrative decision * Psychiatric disorders, disorders of cognitive functions, not allowing the realization of the MRI * Protected adults (subject to a measure of legal protection) or unable to express their consent * Subject with Contraindications to MRI
Where it's running
-
UMR 1214 ToNIC INSERM
Toulouse, France Recruiting
Study contacts
- Principal investigator: Pierre PAYOUX, Pr — Inserm: UMR 1214 ToNIC
- Study coordinator: Nathalie VAYSSIERE, PHD
- Email: nathalie.vayssiere@cnrs.fr
- Phone: +33562746132
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.