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NCT02389257 Clinical Trial

Optically Pumped 4He Magnetometers Performances Compared With Medical Reference Methods (ECG and MEG)

Healthy Clinical Trial

— MINIMAG  

Official title:
Optically Pumped 4He Magnetometers Performances Compared With Medical Reference Methods : Electrocardiography (ECG) and Magnetoencephalography (MEG)

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02389257
Other study ID # MINIMAG
Secondary ID
Status Terminated
Phase Phase 1
First received January 8, 2015
Last updated September 27, 2017
Start date January 2015
Est. completion date September 2017

Study information
Verified date September 2017
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Optically Pumped 4He Magnetometers operability for cerebral and cardiac magnetic fields measurement.

Description:

Optically Pumped 4He Magnetometers vs reference sensors electrocardiogram (ECG) or SQUIDs data acquisitions

Recruitment information / eligibility
Status Terminated
Enrollment 1
Est. completion date September 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- more or equal than 18 years old

- patient affiliated to social security or similarly regime

- informed consent form signed

- without cardiac, neurologic, psychiatric or metabolic medical history.

Exclusion Criteria:

- Pregnant women and lactating mothers

- Ward of court or under guardianship

- Adult unable to express their consent

- Person deprived of freedom by judicial or administrative decision

- Person hospitalized without their consent

- Person under legal protection

- Person with any implant

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• MINIMAG / MEG

• MINIMAG / ECG

Locations
Country Name City State
France CLINATEC Grenoble

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Participants with Adverse EventsMagnetic brain or cardiac activity Measure of Safety and Tolerability 1 year
Secondary Brain or cardiac magnetic activity (Cerebral or cardiac magnetic fields record) Cerebral or cardiac magnetic fields record 1 hour
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