Actively Recruiting
Validation and Implementation of 3T MRI Research Protocols
Led by Institut National de la Santé Et de la Recherche Médicale, France · Updated on 2026-02-18
230
Participants Needed
1
Research Sites
313 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The Philips 3T imager installed on the Pavillon Baudot site is an imager dedicated solely to research. It is not located in hospital premises but in INSERM premises for which an authorization for biomedical research has been granted. This equipment is part of the Technical Platform of the UMR 1214 ToNIC whose main objective is the study of the human brain and the main pathologies that affect it. MRI is an evolving technique, which is used in many research projects. Our technical platform must follow these developments and remain at the cutting edge. One of the essential services of our technical platform is to help set up research protocols and validate acquisition sequences. This development activity is therefore located upstream of research projects involving clinical or fundamental applications. The fact that we can provide our users with a regulatory framework to carry out these development tests for their Research Involving Human Subjects project is a necessity for our research support activity. This study aims to provide a generic framework to test the feasibility of MRI sequences requested within the framework of protocols, but also to optimize MRI acquisition sequences already in place, to improve image quality and reduce artifacts that can degrade the quality of the images obtained. In France, there are just over 35 centers with MRI dedicated to research and therefore with a validation protocol allowing them to validate their sequences.
CONDITIONS
Official Title
Validation and Implementation of 3T MRI Research Protocols
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Persons deprived of liberty by judicial or administrative decision
- Psychiatric disorders or cognitive function disorders that prevent MRI completion
- Protected adults or those unable to express their consent
- Subject with contraindications to MRI
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UMR 1214 ToNIC INSERM
Toulouse, France, 31000
Actively Recruiting
Research Team
N
Nathalie VAYSSIERE, PHD
CONTACT
D
DAGNAC, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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