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Clinical Trials/NCT05767489
NCT05767489RecruitingNot Applicable

Study of Brain Anatomo-functional Substrates Related to the Use of Human Tool by Means of Simultaneous Acquisition of Magnetic Resonance Imaging and Electroencephalogram

IRCCS SYNLAB SDN1 site in 1 country100 target enrollmentStarted: January 18, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Combination of EEG and functional MR (fMRI)

Study Overview

Brief Summary

This is an observational study, conducted on subjects with neurological disorders primarily involving the frontal and parietal lobes of the brain. Throughout the indicated period, the study will aim to enroll 100 subjects divided into 30 units per year. Specifically, the study will be carried out on patients with fronto-parietal dysfunction for whom a prescribed a clinical investigation of electroencephalogram and MRI

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • subjects of either sex with fronto-parietal dysfunction, who are able to able to provide voluntary consent, who have been asked for clinical purposes for an EEG and an MRI

Exclusion Criteria

  • pregnant or presumed pregnant subjects and subjects with claustrophobia or with contraindications to the examination.

Outcomes

Primary Outcomes

Combination of EEG and functional MR (fMRI)

Time Frame: 1-36 months

Interception of differences during simultaneous acquisition related to the variation of action readiness (action readiness) suggested by the visual-perceptual context

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
IRCCS SYNLAB SDN
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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