Development of 3T Magnetic Resonance Research Methods for NIA Studies

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorNational Institute on Aging (NIA)

About this trial

Background:

\- Magnetic resonance imaging (MRI) studies provide important information on the structure and function of various body systems, including the brain, muscles, joints, heart, and blood vessels. Scientific applications of MRI scans often use techniques that need to be modified or refined before they are used in clinical studies. To develop and modify these techniques for the new Philips 3T Achieva whole-body MRI scanner, researchers are interested in conducting trial MRI scans on healthy individuals and individuals with conditions that require imaging studies.

Objectives:

\- To conduct preliminary trials of the 3T MRI facility to develop and refine MRI scanning procedures.

Eligibility:

\- Individuals at least 18 years of age who are able to have magnetic resonance imaging.

Design:

* Participants will be screened with a full medical history and physical examination, as well as blood and urine tests. * Participants will have an MRI scan using the 3T scanner. Some scans may require the use of a contrast agent or radiotracer, which is a small amount of radioactive substance that will be injected before the start of the scan. Some participants may be asked to perform tasks of thinking and movement while in the scanner, in order to test the procedures required for a functional MRI scan. * No treatment will be provided as part of this protocol.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Ability of subject to understand the study and stated willingness to comply with all study procedures.

Male or female, age > 18years.

Able to speak and read English.

Capable of providing informed consent.

Disqualifiers

Has condition and/or non-removable device contraindicated for MRI as per the MRI eligibility form.

Weight > 300lbs (MRI scanner weight limit)

Is currently pregnant or a nursing mother.

Trial population

Healthy volunteers, male and female, 18yrs and older

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

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

Trial outcomes

Primary outcomes

1

Develop and refine scanning procedures

To develop and refine specific imaging and spectroscopic methods.

Time frame
2 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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