Development of New Software Capabilities for Use With Cardiovascular Magnetic Resonance Imaging
Terminated
- Conditions
- Abnormalities, Cardiovascular
- Registration Number
- NCT00593541
- Lead Sponsor
- University of California, Davis
- Brief Summary
This Protocol is intended to facilitate development and testing of new cardiovascular MRI software capabilities by UC Davis Research Faculty, as well as to facilitate the evaluation of new software capabilities provided by GE and Siemens.
- Detailed Description
This protocol will permit normal subjects, as well as patients with suspected or proven medical conditions, to undergo MRI studies using the new software capabilities. This Protocol is not restricted to imaging of a particular organ system or disease. The Protocol does not involve injection of any contrast agent, or other minimally-invasive or invasive procedure. It is intended only for those cases for which the only requirement of the subject is to relax and lie still while imaging is being performed.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
- 18 years of age or older
- Ability to give informed, written consent
- Not Pregnant or breastfeeding
Exclusion Criteria
- Electrically, magnetically, or mechanically activated implants (for example, cardiac-pacemakers)
- Ferromagnetic implant, such as an aneurysm clip, surgical clip, or prosthesis
- History of uncontrolled claustrophobia
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Extend or generalize certain capabilities, such as new data acquisition pulse sequences, new image processing and analysis software for structural and functional analysis of the MR images Post-scanning
- Secondary Outcome Measures
Name Time Method Improve image quality by various techniques (e.g. reducing the effects of motion) Post-scanning