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

NCT ID: NCT05767489

Last Updated: 2024-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-18

Study Completion Date

2025-01-17

Brief Summary

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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

Detailed Description

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Conditions

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Patients With Frontal and Parietal Lobe Dysfunction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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electroencephalogram (EEG) and magnetic resonance (MR)

High-resolution 3D T1 and T2 sequences, acquired in the sagittal plane and MR reconstructed in the remaining orthogonal planes, for morphological assessment of different cortical and subcortical.

EEG tracing involving recording channels such as eye tracking (eye-tracking: electrooculogram, pupillometry, saccades, fixation times on areas predefined areas), performance measures (response times), electrocardiogram and electromyogram proper to clinical acquisition

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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IRCCS SYNLAB SDN

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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IRCCS Synlab SDN

Naples, , Italy

Site Status RECRUITING

Countries

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Italy

Facility Contacts

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Laura Pierri, MSC

Role: primary

0812408470

Other Identifiers

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8/20

Identifier Type: -

Identifier Source: org_study_id

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