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OpenTrials
Completed

NCT Number: NCT03152539

Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Healthy Volunteers

The main objective of the studies that will be carried out on volunteer patients who have given their consent will be the development and optimization of the sequence parameters or the design of the stimulation paradigms in order to optimize the quality and Relevance of the images realized taking into account anatomical, functional or metabolic parameters. These adjustments will be carried out without interfering with the management of voluntary patients

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Grenoble-Alpes

Grenoble, 38043, France

About this study

The pathologies that interest us in these refinements concern mainly the chronic (or sequellar) brain disorders which can be degenerative, developmental or vascular. The patients who will be recruited will be known patients of our Service (University Clinic of Neuroradiology and MRI) that we follow during checks. The type of examination that will be applied to them, between MRI, EEG and NIRS, will be specified in the consent form. These examinations will not be invoiced either to the patient or to the social security, and the related costs will be borne by our Federative Research Structure or sometimes, when these explorations are upstream of a defined research protocol and funded, They will be financed under this protocol.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • major
  • socially insured persons
  • given their consent.
  • absence of contraindication to the MRI examination

Exclusion criteria

  • Subjects under the age of 18
  • pregnant women
  • all other persons referred to in articles L1121-5 to L1121-8 of the CSP

Treatment and study plan

MRI

Radiation

EEG

Device

NIRS

Device

Primary outcomes

  1. Spatial resolution of new MRI imaging sequences MRI scanning.

    Time frame: Two hours

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Registry information

Acronym: MAP-VS

Important dates

Study start
2012
Primary completion
2021
Study completion
2021
First posted
May 15, 2017
Registry last updated
Oct 20, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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