RECRUITING

Evaluation and Optimization of Ultrasound and/or MRI Hardware and Software

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Evaluation and Optimization of Ultrasound and/or MRI Hardware and Software in Existing SUNY Ultrasound and/or MRI Units and Newly Installed Commercially Available Units

Quick Facts

Study Start:2007-10
Study Completion:2030-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT00640107

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Able to Understand and Sign Informed Consent Disclosure (ICD)
  2. * Healthy Volunteers Aged 18-70
  3. * Healthy Volunteers with No History of Aneurysm Clips, Cardiac Pacemakers, Claustrophobia, Neurostimulators, and Pregnancy.
  1. * Subjects \> 300 Pounds
  2. * Subjects \< 18 Years Old
  3. * Subjects \> 70 Years Old
  4. * Subjects w/ Aneurysm Clips
  5. * Subjects w/ Cardiac Pacemakers
  6. * Subjects w/ Claustrophobia
  7. * Subjects w/ Neurostimulators
  8. * Subjects w/ Pregnancy

Contacts and Locations

Study Contact

Donna Bolourchi, BSc
CONTACT
(315) 464-7424
bolourcd@upstate.edu
Kyra Crossett, BSc
CONTACT
(315) 464-5098
crossetk@upstate.edu

Principal Investigator

Marzieh Nezamzadeh, PhD
PRINCIPAL_INVESTIGATOR
State University of New York - Upstate Medical University

Study Locations (Sites)

SUNY Upstate Medical University
Syracuse, New York, 13210
United States

Collaborators and Investigators

Sponsor: State University of New York - Upstate Medical University

  • Marzieh Nezamzadeh, PhD, PRINCIPAL_INVESTIGATOR, State University of New York - Upstate Medical University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2007-10
Study Completion Date2030-09

Study Record Updates

Study Start Date2007-10
Study Completion Date2030-09

Terms related to this study

Keywords Provided by Researchers

  • Magnetic Resonance Imaging
  • Ultrasound

Additional Relevant MeSH Terms

  • Healthy