Skip to main content
Clinical Trials/NCT02186054
NCT02186054TerminatedNot Applicable

Enhancement of T2 Weighted Imaging of the Liver With Fast Spin Echo Magnetic Resonance Imaging (MRI).

Ottawa Hospital Research Institute1 site in 1 country50 target enrollmentStarted: June 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
50
Locations
1
Primary Endpoint
The number of abdominal MRI scans deemed improved quality

Study Overview

Brief Summary

The purpose of this study is to test two new MRI (magnetic resonance imaging) sequences to see how they compare to previously used imaging sequences as they may improve the quality of abdominal MRI.

Detailed Description

  • Approximately 50 patients undergoing routine liver MRI in our practice imaged with one of our 4 clinical scanners will undergo our standard liver MRI protocol with the addition of 2 breath-hold sequences (FSE Flex and eSSFSE) only increasing the scan time by approximately 3 minutes.
  • Data will be retrieved from examinations that have been performed from the patient's electronic imaging file stored in our picture archiving and communication system (PACS).
  • Images will be completely anonymized. No patient identifiers will be available on the images during the analysis.
  • Analyses will include the visual assessment of image quality, presence and severity of imaging artifact and other non-invasive imaging outcomes performed by radiologists blinded to patient information and the type of sequence performed. Data will be presented in a Likert type scale (1=poor, 2=suboptimal, 3=average, 4=above average and 5=excellent) and imaging parameters will be compared using the Wilcoxon sign rank test.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
Single (Investigator)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients undergoing routine liver MRI imaged with one of our 4 clinical scanners (MR 750W, General Electric, Milwaukee WI)

Exclusion Criteria

  • •Patients not undergoing routine liver MRI

Arms & Interventions

Imaging- MRI examinations

Other

Liver MRI imaging will be performed on 50 patients.

Intervention: MRI examinations (Device)

Outcomes

Primary Outcomes

The number of abdominal MRI scans deemed improved quality

Time Frame: Regular scan time with one of 4 clinical scanners plus 3 additional minutes

Data is presented in a Likert type scale (1=poor, 2=suboptimal, 3=average, 4=above average and 5=excellent) and imaging parameters are compared using the Wilcoxon sign rank test.

Secondary Outcomes

  • The number of MRI scans that display severity of imaging artifact(Regular scan time with one of 4 clinical scanners plus 3 additional minutes)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials