Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound
Primary Purpose
Breast Diseases
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Supine automated breast ultrasound scanner
High-resolution handheld breast ultrasound
Sponsored by
About this trial
This is an interventional diagnostic trial for Breast Diseases
Eligibility Criteria
Inclusion Criteria:
- anyone who is referred for an ultrasound of the breast
Exclusion Criteria:
- Subjects whose breast thickness is greater than 6 cm.The maximum depth of image filed for the ABVS acquisition is 6 cm
Sites / Locations
- Northwestern Medicine
- Weinstein Imaging
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Automated & Handheld breast US exams
Arm Description
Automated breast ultrasound exam: 3D supine automated breast ultrasound scanner. Handheld breast ultrasound exam: High-resolution handheld breast ultrasound.
Outcomes
Primary Outcome Measures
Ratio of Lesions Detected With Automated Breast Ultrasound (ABVS) Compared to the Standard of Care Handheld (HH) Breast Ultrasound (US)
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
Secondary Outcome Measures
Full Information
NCT ID
NCT02310776
First Posted
November 25, 2014
Last Updated
January 7, 2016
Sponsor
Northwestern University
Collaborators
Siemens Medical Solutions
1. Study Identification
Unique Protocol Identification Number
NCT02310776
Brief Title
Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound
Official Title
Breast Lesion Detection Using the Acuson S2000 Automated Breast Volume Scanner (ABVS) Compared With Handheld (HH) Physician-performed Ultrasound (US) Examinations
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
October 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
Collaborators
Siemens Medical Solutions
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Diseases
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
501 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Automated & Handheld breast US exams
Arm Type
Other
Arm Description
Automated breast ultrasound exam: 3D supine automated breast ultrasound scanner.
Handheld breast ultrasound exam: High-resolution handheld breast ultrasound.
Intervention Type
Device
Intervention Name(s)
Supine automated breast ultrasound scanner
Intervention Description
Automated wide-field-of-view breast ultrasound volume scan performed by a sonographer and interpreted by a breast imaging radiologist.
Intervention Type
Device
Intervention Name(s)
High-resolution handheld breast ultrasound
Intervention Description
Standard of care, small field-of-view 2D breast ultrasound performed and interpreted by a breast imaging radiologist
Primary Outcome Measure Information:
Title
Ratio of Lesions Detected With Automated Breast Ultrasound (ABVS) Compared to the Standard of Care Handheld (HH) Breast Ultrasound (US)
Description
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
Time Frame
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.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
anyone who is referred for an ultrasound of the breast
Exclusion Criteria:
Subjects whose breast thickness is greater than 6 cm.The maximum depth of image filed for the ABVS acquisition is 6 cm
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ellen B Mendelson, MD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern Medicine
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Weinstein Imaging
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15206
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Lesion Detection of Automated Breast Ultrasound Compared With Handheld Physician-performed Breast Ultrasound
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