Preparation and Feasibility of Exams for Expected Studies
Recruiting · NCT05698810 · Interventional (participants receive a specific treatment) · Lead sponsor: University Hospital, Grenoble
View the official record on ClinicalTrials.gov →Interventions studied
CE marked Medical Device ElectroCardioGraphy (ECG) usabilityCE marked Medical Device ElectroEncephaloGraphy (EEG) usabilityCE marked Medical Device Magnetic Resonance Imaging (MRI) usabilityCE marked Medical Device MagnetoEncephaloGraphy (MEG) usability
What this trial is about
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 ...)
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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.
Where it is running
1 location listed.
- Clinatec Cea/Chuga - Grenoble, France