Magnetic Resonance Imaging of Human Biometrics

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02942667

Acronym

MRI HB

Enrollment

Registered

2016-10-24

Start date

2016-08-31

Completion date

2018-02-02

Last updated

2018-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Volunteers

Brief summary

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

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

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

Exclusion criteria

* 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 * Subject has magnetizable implant * Subject requires legally authorized representative to sign Patient Informed Consent (PIC)/ Informed Consent (IC) form * Subject has other contraindication for an MRI scan as defined by the study site

Design outcomes

Primary

Measure	Time frame
Collect High Quality MRI Data	Approximately 6 Weeks

Countries

United States

Outcome results