Magnetic Resonance Imaging of Human Biometrics

Completed

Conditions studied: Volunteers

In brief

The primary objective is to collect high quality MRI data (un-processed or processed) from participating subjects for Medtronic research purposes.

Key facts

Study ID

NCT02942667

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

12

Starts

2016-08-01

Expected to finish

2018-02-02

Last updated by the study team

2018-02-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subject is at least 18 years of age
• Subject is willing and able to undergo study requirements

You may not qualify if…

• Subject has a medical condition that precludes the subject from participation
• Subject has any magnetizable foreign object (e.g. jewelry) which cannot be removed for the duration of the study
• Subject is claustrophobic
• Subject is unable to stand without assistance
• Subject requires sedation for MRI scans
• Subject is implanted with non-Magnetic Resonance conditional or other medical device:
• Non-MRI conditional pacemaker, Implantable Cardiac Defibrillator (ICD), Cardiac Resynchronization Therapy (CRT), or an implantable hemodynamic monitor
• Metal clips (i.e. brain aneurysm clip)
• Artificial heart valve
• Implanted neural stimulator
• Gastric capsule camera
• Swan Ganz catheter
• Stent
• Inferior Vena Cava (IVC) filter
• Orthopedic implant
• Eye prosthesis
• Vascular access port
• Penile prosthesis
• Intrauterine device
• Subject has a cochlear implant, middle ear prosthesis, or has had ear surgery
• Subject has ocular foreign bodies (i.e. metal shavings)
• Subject has any type of device held in place by a magnet (i.e. dentures)
• Subject has an insulin pump
• Subject has metal shrapnel
• Subject is pregnant or lactating

Where it is running

• Study site — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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