Imaging Techniques in MRI

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorNational Institutes of Health Clinical Center (CC)

About this trial

Background:

\- Magnetic resonance imaging (MRI) scans must be performed according to specified sets of parameters that provide optimal images of each organ and each area of the body. These scanning parameters are often specific to the institution or organization at which they are employed, and may also depend on the manufacturer of the MRI scanning equipment. Because MRI scanning equipment is always being updated and upgraded, researchers are interested in developing new and optimized scanning parameters for MRI scans.

Objectives:

\- To improve current methods and develop new techniques for magnetic resonance imaging.

Eligibility:

* Individuals 18 years of age and older who are either volunteers or current NIH protocol participants. * Participants must not have any medical history factors (e.g., extreme claustrophobia, history of metal implants) that would prevent them from receiving MRI scans.

Design:

* Participants will have at least one MRI scan that will last from 20 minutes to 2 hours (most scans will last between 45 and 90 minutes). The total time commitment for most visits will be approximately 4 hours from start to finish. * Some MRI techniques require standard monitoring equipment or specific procedures during the scanning, such as an electrocardiogram. * Participants will have blood samples taken at the time of the scan. Some MRI studies will require the use of a contrast agent that will be administered during the scan. * Volunteers may be asked to return for additional MRI scans over the course of a few years. Follow-up scans may be done on the same part of the body or on different parts of the body. No more than one MRI scan will be performed in any 4-week period for this protocol....

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Aneurysm clip, implanted neural stimulator,

Implanted cardiac pacemaker, defibrillator, or certain other implanted electrical or metallic devices,

Cochlear implant, ocular foreign body (metal shavings),

Any implanted device (pumps, infusion devices, etc.),

Trial population

Volunteers (maybe Volunteers, NIH employee and current NIH protocol participants)

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,000 Participants
are grouped into 1 trial group
Group A: Volunteers

Trial outcomes

Primary outcomes

1

To refine current methodology and develop new techniques for MRI

To refine current methodology and develop new techniques for magnetic resonance imaging in the general population.

Time frame
End of study

Secondary outcomes

Other outcomes

Sponsors and contacts

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