Evaluation of the Signa Excite 3.0 T MRI Excite for Detection and Characterization of Liver Lesions

NCT00527891 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2012-07-31

No results posted yet for this study

Summary

Primary Objective:

1\. To compare the efficacy of 1.5T vs. 3T T1 and T2-weighted MR images sequences for the detection and evaluation of liver lesions.

Conditions

Interventions

PROCEDURE

Signa Excite 3.0 T MRI Scan

Signa Excite 3.0 T MRI scan within a two week period from the date of receiving standard 1.5 T MR of the liver area.

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Janio Szklaruk, MD · M.D. Anderson Cancer Center

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-06-30
Primary Completion
2007-09-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00527891 on ClinicalTrials.gov