Adjustment Exploratory Protocols and Functional Evaluation of New Non Invasive Devices in Healthy Volunteers

Not Applicable

Completed

• Conditions: Healthy Volunteers
• Interventions: Device: Imaging devices; Device: New Non Invasive Devices

• Registration Number: NCT02790411
• Lead Sponsor: University Hospital, Grenoble

Brief Summary

Parameters, sequences or paradigms optimisation in view of data quality and relevancy improvement.

Detailed Description

Various tests are needed for methodological optimization of the several devices (per-operative MRI, MEG, EEG, SPECT-CT, motor platform) of the technological platform.

Study Timeline

• Study Start: 2013-05-21
• Study First Submitted: 2016-05-12
• Study First Submitted QC: 2016-05-30
• Study First Posted: 2016-06-03
• Primary Completion: 2021-05-21
• Study Completion: 2021-05-21
• Status Verified: 2022-11
• Last Update Submitted: 2022-11-08
• Last Update Posted: 2022-11-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 96

Inclusion Criteria

• Healthy volunteers
• Male or female aged over 18 years
• Registered in the French social security scheme
• Signed informed consent

Exclusion Criteria

• Contraindication to Magnetoencephalography (MEG) and/or Electroencephalography (EEG)
• Contraindication to Magnetic resonance imaging (MRI)
• All categories of protected persons

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
healthy volunteers	Imaging devices	Imaging devices New Non Invasive Devices
healthy volunteers	New Non Invasive Devices	Imaging devices New Non Invasive Devices

Primary Outcome Measures

Name	Time	Method
Electrical brain activity	2 hours	EEG records
Magnetic brain activity	2 hours	MEG records
Motor activity parameters	2 hours	Motor platform records
Brain imaging	2 hours	MRI and SPECT-CT records

Trial Locations

Locations (1)

CLINATEC; 🇫🇷 Grenoble, France