Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Voluntary Patients
MAP-PV
1 other identifier
interventional
48
1 country
1
Brief Summary
Studies that will be carried out on healthy volunteers will have as main objective the development and optimization of the parameters of sequences or the design of the paradigms of stimulation in order to optimize the quality and the relevance of the images realized taking in Taking account of anatomical, functional or metabolic parameters, or integrating new approaches resulting from technical evolutions
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2013
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2013
CompletedFirst Submitted
Initial submission to the registry
April 24, 2017
CompletedFirst Posted
Study publicly available on registry
May 19, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 8, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
July 8, 2021
CompletedOctober 20, 2021
October 1, 2021
8.4 years
April 24, 2017
October 19, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Spatial resolution of new MRI imaging sequences MRI scanning.
Two hours
Study Arms (3)
Development of MRI protocols
EXPERIMENTALMRI exam to grade differents interventions for future research
Development of EEG protocols
EXPERIMENTALEEF exam to grade differents interventions for future research
Development of NIRS protocols
EXPERIMENTALNIRS exam to grade differents interventions for future research
Interventions
Eligibility Criteria
You may qualify if:
- major voluntary patients
- socially insured.
- Karnofsky score above 60%.
- given their consent.
- absence of contraindication to the MRI examination
You may not qualify if:
- Subjects under the age of 18
- pregnant women
- persons referred to in articles L1121-5 to L1121-8 of the CSP.
- Patients with acute illness
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Grenoble-Alpes
Grenoble, 38043, France
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Masking Details
- Magnetic resonance imaging
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 24, 2017
First Posted
May 19, 2017
Study Start
February 1, 2013
Primary Completion
July 8, 2021
Study Completion
July 8, 2021
Last Updated
October 20, 2021
Record last verified: 2021-10
Data Sharing
- IPD Sharing
- Will not share