Evaluate the diagnostic accuracy of the Planmed Sophie Nuance Full Field Digital Mammography (FFDM) X-ray System compared to screen-film mammography (SFM) in the detection of breast cancer.
Objectives: 1) To establish the non-inferiority of the diagnostic accuracy of the Planmed Sophie Nuance Full Field Digital Mammography (FFDM) X-ray System compared to screen-film mammography (SFM) in the detection of breast cancer; and 2) To demonstrate in a comparative side-by-side feature analysis that interpretations based on the Planmed Sophie Nuance FFDM X-ray System are diagnostically non-inferior to SFM in the detection of breast cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
250
Full Field Digital Mammogram
Mroz-Baier Breast Care Clinic
Memphis, Tennessee, United States
The Rose
Houston, Texas, United States
Area under ROC curve based on subjects' maximum POM scores; sensitivity based on subjects' maximum BI-RADS scores with 4 or higher as positive for cancer; and specificity based on subjects maximum BI-RADS scores with 4 or higher as positive for cancer
Time frame: Approximately one year after completion of study.
area under the ROC curve based on the maximum POM score per subject-breast
Time frame: Approximately one year after completion of study.
area under the ROC curve based on the POM scores from the ten regions of a subject's breasts;
Time frame: Approximately one year after completion of study.
sensitivity based on subjects' maximum BI-RADS scores using a cut-point of 3 or higher as positive for cancer;
Time frame: Approximately one year after completion of study.
specificity based on subjects' maximum BI-RADS scores using a cut-point of 3 or higher as positive for cancer;
Time frame: Approximately one year after completion of study.
Sensitivity and specificity based on the maximum BI-RADS scores per subject-breast using 4 or higher for positive; and sensitivity and specificity based on the maximum BI-RADS scores per subject-breast using 3 or higher for positive.
Time frame: Approximately one year after completion of study.
Feature Analysis Study; side by side assessment of SFM and FFDM images and comparison of quality features: lesion conspicuity, tissue visibility at chest wall, tissue visibility at skin line, axillary details (MLO), overall contrast, overall sharpness
Time frame: Approximately one year after completion of study.
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Adverse event assessment
Time frame: Approximately 24 hours after completion of FFDM