Syngo NATIVE Contrast Enhanced 3D MRA on 3T Verio Magnet

Status Completed

Clinical Trial Summary

The purpose of the study is to compare non-contrast abdominal MR Angiogram (MRA) syngo NATIVE sequence performed on a 3T Verio Siemens magnet to a standard contrast-enhanced MRA performed as part of routine clinical care in patients with normal renal function to determine if the non-contrast NATIVE sequence is a viable alternative to contrast enhanced MRA in patients with renal insufficiency. There are no interventions--this is an observational study.

Clinical Trial Description

If the NATIVE sequence proves to be a viable alternative to contrast enhanced MRA it will provide imaging physicians with the diagnostic tool to assess vascular disease in patients with renal insufficiency without placing them at risk for additional co-morbidities. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02065648
Study type	Observational
Source	Cedars-Sinai Medical Center
Contact
Status	Completed
Phase	N/A
Start date	May 2012
Completion date	March 2015

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