About this trial
The purpose of this study is to evaluate and optimize ultrasound and/or MRI hardware and software in both existing ultrasound/MRI units as well as in newly installed commercially available ultrasound/MRI units. The study also serves to familiarize the ultrasound/MRI technician staff with how to operate newly installed software sequences or hardware. The information obtained from this study will be utilized to optimize new software sequences and hardware that have been installed on the UMU ultrasound/MRI scanners. This will offer ultrasound/MRI technologists ample time to become familiar with the operation of new equipment. More specifically, the objectives of this study are to maximize contrast to noise (CNR) and signal to noise (SNR) ratios for new imaging sequences and hardware to obtain high quality images, maximize the potential of new machines and associated software/hardware to obtain the highest quality of images, and obtain the highest quality images in reasonable scan time to minimize patient motion.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Able to Understand and Sign Informed Consent Disclosure (ICD)
Healthy Volunteers Aged 18-70
Healthy Volunteers with No History of Aneurysm Clips, Cardiac Pacemakers, Claustrophobia, Neurostimulators, and Pregnancy.
Disqualifiers
Subjects > 300 Pounds
Subjects < 18 Years Old
Subjects > 70 Years Old
Subjects w/ Aneurysm Clips
Trial population
The study population is comprised of healthy volunteers aged 18-70 who are able and willing to sign an informed consent disclosure (ICD) form to undergo an MRI scan if they meet all screening criteria.
Trial design
Case-only
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
This trial has no outcomes listed.Sponsors and contacts
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