Preparation and Feasibility of Exams for Expected Studies

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

RECRUITING

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-20

Study Completion Date

2033-03-20

Brief Summary

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Feasibility study: the examinations carried out as part of this protocol aim to carry out all the acquisitions and simulations of use, necessary for the development of the clinical research protocols to come to Clinatec (in particular, configuration of the equipment, dimension of the examination time and the size of the cohorts etc ...)

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Detailed Description

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To ensure the feasibility of a clinical trial, it is necessary to test the parameters as well as the sequence of the different examination times offered to participants.

The expected results of this protocol are mainly the dimension of experimental paradigms and the optimization of the clinical management of subjects.

Conditions

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Healthy Volunteers Parkinson's Disease Patients Para/Tetraplegic Patients

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

volunteers

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Healthy Volunteers

tests

Group Type OTHER

CE marked Medical Device MagnetoEncephaloGraphy (MEG) usability

Intervention Type OTHER

tests

CE marked Medical Device Magnetic Resonance Imaging (MRI) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroEncephaloGraphy (EEG) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroCardioGraphy (ECG) usability

Intervention Type OTHER

tests

Parkinson's Disease patients

tests

Group Type OTHER

CE marked Medical Device MagnetoEncephaloGraphy (MEG) usability

Intervention Type OTHER

tests

CE marked Medical Device Magnetic Resonance Imaging (MRI) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroEncephaloGraphy (EEG) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroCardioGraphy (ECG) usability

Intervention Type OTHER

tests

Para/tetraplegic Patients

tests

Group Type OTHER

CE marked Medical Device MagnetoEncephaloGraphy (MEG) usability

Intervention Type OTHER

tests

CE marked Medical Device Magnetic Resonance Imaging (MRI) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroEncephaloGraphy (EEG) usability

Intervention Type OTHER

tests

CE marked Medical Device ElectroCardioGraphy (ECG) usability

Intervention Type OTHER

tests

Interventions

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CE marked Medical Device MagnetoEncephaloGraphy (MEG) usability

tests

Intervention Type OTHER

CE marked Medical Device Magnetic Resonance Imaging (MRI) usability

tests

Intervention Type OTHER

CE marked Medical Device ElectroEncephaloGraphy (EEG) usability

tests

Intervention Type OTHER

CE marked Medical Device ElectroCardioGraphy (ECG) usability

tests

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age ⩾ 18 years
* Affiliated to a social security scheme
* Free and informed consent signed

Exclusion Criteria

* Subject in a period of exclusion from another study.
* Subject deprived of liberty by a judicial or administrative decision, or major subject subject to a legal protection measure (guardianship, curatorship and safeguarding of justice) referred to in Articles 1121-6 to 1121-8 of the Public Health Code.
* Subject who would receive more than 4500 euros in compensation because of his participation in other research involving the human person in the 12 months preceding this study.
* Pregnant woman, parturient, nursing mother (Article 1121-5 of the Public Health Code)
* Subject not reachable urgently.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes