Development of New Software Capabilities for Use With Cardiovascular Magnetic Resonance Imaging

Abnormalities, Cardiovascular Clinical Trial

— CVMRI  

Official title:

Development of New Software Capabilities for Use With Cardiovascular Magnetic Resonance Imaging

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00593541
• Other study ID #: 200210689
• Status: Terminated
• Phase: N/A
• First received: January 3, 2008
• Last updated: May 24, 2017
• Start date: May 1999
• Est. completion date: July 2014

Study information

• Verified date: May 2017
• Source: University of California, Davis
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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 information / eligibility

• Status: Terminated
• Enrollment: 42
• Est. completion date: July 2014
• Est. primary completion date: July 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Abnormalities, Cardiovascular
• Cardiovascular Abnormalities

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of California, Davis

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	Improve image quality by various techniques (e.g. reducing the effects of motion)		Post-scanning