Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound

Not Applicable

Completed

• Conditions: Breast Diseases
• Interventions: Device: Supine automated breast ultrasound scanner; Device: High-resolution handheld breast ultrasound

• Registration Number: NCT02310776
• Lead Sponsor: Northwestern University

Brief Summary

Compare lesion detection of the automated breast ultrasound (ABVS) exam with the conventional handheld (HH) breast ultrasound (US) exam.

Detailed Description

This is a research study to test a FDA-approved automated breast ultrasound (ABVS) machine in subjects recommended for an ultrasound of the breast. The main purpose of the study is to compare images obtained from the automated breast ultrasound exam with the standard physician performed handheld breast ultrasound exam for lesion detection equivalence.

Each subject will have a bilateral hand-held breast ultrasound and a bilateral automated breast ultrasound, both exams preferably done on the same day. The hand-held ultrasound will be performed by a breast imaging physician participating in the study and the automated ultrasound exam will be performed by a sonographer.

There is no radiation risk from ultrasound. The physician performing the handheld breast ultrasound is blinded to the study, will not know the subject's history, but only the reason for the breast ultrasound exam.

The automated scan requires gentle pressure on the breast during a scan. Three basic views will be acquired for each breast, each scan lasting approximately one minute. Once all necessary views are acquired, the images will be sent to a remote workstation, where a second radiologist, also blinded to the results of the handheld study, will interpret the automated ultrasound.

Once all images and patient information are gathered, the study radiologists will review the previous images, if available, to provide the final result that will determine clinical management. Therefore, it is possible that the hand-held or automated ultrasound scan will lead to further evaluation of the breast and possibly a biopsy.

Study Timeline

• Study Start: 2012-06
• Primary Completion: 2014-03
• Study First Submitted: 2014-11-25
• Study First Submitted QC: 2014-12-04
• Study First Posted: 2014-12-08
• Results First Submitted: 2015-04-21
• Results First Submitted QC: 2015-04-21
• Results First Posted: 2015-05-08
• Study Completion: 2015-10
• Status Verified: 2016-01
• Last Update Submitted: 2016-01-07
• Last Update Posted: 2016-02-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 501

Inclusion Criteria

• anyone who is referred for an ultrasound of the breast

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Exclusion Criteria

• Subjects whose breast thickness is greater than 6 cm.The maximum depth of image filed for the ABVS acquisition is 6 cm

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Automated & Handheld breast US exams	High-resolution handheld breast ultrasound	1. Automated breast ultrasound exam: 3D supine automated breast ultrasound scanner. 2. Handheld breast ultrasound exam: High-resolution handheld breast ultrasound.
Automated & Handheld breast US exams	Supine automated breast ultrasound scanner	1. Automated breast ultrasound exam: 3D supine automated breast ultrasound scanner. 2. Handheld breast ultrasound exam: High-resolution handheld breast ultrasound.

Primary Outcome Measures

Name	Time	Method
Ratio of Lesions Detected With Automated Breast Ultrasound (ABVS) Compared to the Standard of Care Handheld (HH) Breast Ultrasound (US)	Time for performance of ABVS was measured separately from interpretation time. Time for performance of real time HH whole breast US was also measured. For HH US physician performed, performance included interpretation.	Solid lesions found on whole breast 3D supine automated breast ultrasound are compared in number and identity with solid lesions found using high resolution standard of care handheld breast ultrasound performed by physicians

Trial Locations

Locations (2)

Northwestern Medicine; 🇺🇸 Chicago, Illinois, United States

Weinstein Imaging; 🇺🇸 Pittsburgh, Pennsylvania, United States