Evaluation and Optimization of Ultrasound and/or MRI Hardware and Software
1 other identifier
observational
30
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2007
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2007
CompletedFirst Submitted
Initial submission to the registry
March 12, 2008
CompletedFirst Posted
Study publicly available on registry
March 20, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2030
June 28, 2024
June 1, 2024
18.9 years
March 12, 2008
June 27, 2024
Conditions
Keywords
Eligibility Criteria
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.
You may qualify if:
- 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.
You may not qualify if:
- Subjects \> 300 Pounds
- Subjects \< 18 Years Old
- Subjects \> 70 Years Old
- Subjects w/ Aneurysm Clips
- Subjects w/ Cardiac Pacemakers
- Subjects w/ Claustrophobia
- Subjects w/ Neurostimulators
- Subjects w/ Pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
SUNY Upstate Medical University
Syracuse, New York, 13210, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Marzieh Nezamzadeh, PhD
State University of New York - Upstate Medical University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Diagnostic Radiology Physicist
Study Record Dates
First Submitted
March 12, 2008
First Posted
March 20, 2008
Study Start
October 1, 2007
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2030
Last Updated
June 28, 2024
Record last verified: 2024-06
Data Sharing
- IPD Sharing
- Will not share
De-identified data will be the only information available for sharing purposes.