Developing MRI protocols and neuro-physiological measurements

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project focuses on enhancing MRI technology by optimizing sequence parameters and designing stimulation paradigms for both healthy individuals and patients. The aim is to improve the quality and relevance of MRI images while considering anatomical, functional, and metabolic parameters. Participants will undergo MRI scans and additional physiological measurements to assess the effectiveness of the new protocols. The study will ensure that all procedures are conducted with informed consent and adherence to safety protocols.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Participants with normal or corrected vision
* Participants affiliated to a social security scheme or beneficiaries of such a scheme
* Participants with French as their mother tongue
* Participants who have given the signed informed consent before carrying out any procedure related to the study.
* Volunteer patients will be recruited as part of their follow-up at the CHU. Their pathology will be in agreement with that of the research protocol to be optimized.

Exclusion Criteria:

Criteria relating to contraindications to the explorations provided for by the MRI protocol:

* metallic glitter in the eyes
* retinal operation
* claustrophobia
* wearer of pacemaker or cardiac defribrillator or vascular clip or prosthesis cardiac or insulin pump or implanted device to deliver medication or hearing implant or prosthesis or vascular shunt or paragraph or screws, plate metal or tattoo or piercing or implanted metal object or lead shot hunt

  * Alcohol ingestion before the examination
  * Pregnant, lactating and parturient women
  * Major protected by law
  * Participants under administrative or judicial supervision
  * Participation in another ongoing study if the study may interfere with participation in the protocol MAP-IRMaGe.

Where it's running

• Unité Mixte de Service IRMaGe US 017
  La Tronche, France Recruiting

Study contacts

• Study coordinator: ATTYE ARNAUD, MD, PhD
• Email: aattye@chu-grenoble-alpes.fr
• Phone: 4 76 76 57 39

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.