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Spots Global Cancer Trial Database for The Prone to Supine Breast MRI Trial

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: The Prone to Supine Breast MRI Trial

Official Title: The Prone to Supine Breast MRI Trial

Study ID: NCT03573804

Conditions

Breast Cancer

Interventions

Prone to Supine MRI

Study Description

Brief Summary: The purpose of this study is to determine whether a supine MRI obtained immediately after a standard diagnostic prone MRI exam, without a second injection of gadolinium (Gd) contrast material, would be of sufficient quality to allow the Radiologist to define the tumor edges ("segment" the tumor) so that a 3-D image of the tumor can be generated to form a BCL.

Detailed Description: The purpose of this study is to find out whether additional MRI images taken with patients in a different position after completing a standard MRI are of sufficient quality to allow a radiologist to identify the edges of the tumor. These additional MRI images will only take about 10-15 minutes to obtain and will not require a second injection of contrast material.The information gathered in this study will make it more feasible to use a new device called the "breast cancer locator" to help surgeons more accurately remove breast cancers.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States

Contact Details

Name: Timothy B Rooney, MD

Affiliation: Dartmouth-Hitchcock Medical Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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