The PET/MR device components and accessories are under development in order to optimize, validate and improve the design including improving the quality of images. The purpose of this study is: * Aim 1: Perform iterative evaluations of the device (including features and components) to optimize device performance and assess feasibility of new features; * Aim 2: Perform activities in support of design validation as needed for regulatory submission; * Aim 3: Evaluate device complaints and analyze potential causes.
This is a non-randomized, non-statistically powered, single-site, prospective study designed to gather imaging data for design optimization, regulatory submission and future product development of an investigational hybrid PET/MRI scanner. Subjects will undergo a clinically indicated PET/CT exam subsequent to tracer administration. Once clinical imaging is complete, subjects will be transported to the PET/MR scanner at the General Electric (GE) Facility for additional imaging. No additional pharmaceuticals or ionizing radiation will be utilized as part of this study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
4
GE PET/MRI system
Froedtert Hospital
Milwaukee, Wisconsin, United States
PET/MR Scan Obtained
One PET/MR scan per subject should be obtained. The scan images are evaluated by a subject matter expert for adequate diagnostic quality.
Time frame: One (1) day
Device Complaints
Number of device complaints reported during a scan
Time frame: One day
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