Transpara in RCTs
The only Breast AI solution selected by randomised controlled trials
Randomised controlled trials (RCTs) are the gold standard in clinical evidence. Transpara Detection is the only solution selected to be part of randomised controlled trials, including initiatives currently underway in Sweden, Norway, and the United States.
MASAI - Sweden
PRISM - USA
AIMS - Norway
Sweden's MASAI trial found a 29% increase in cancer detection and a 44% decrease in screen-reading workload when incorporating Transpara Detection compared to a double-reading standard of care. Hernström, et al., 2025, The Lancet Digital Health
MASAI - Sweden
PRISM - USA
5 years, 50-60 sites,
~120 radiologists, 400k exams
The first Breast AI RCT to focus on the United States, the PRISM Trial (Pragmatic Randomized Trial of Artificial Intelligence for Screening Mammography) is supported by a $16 million award from the Patient-Centered Outcomes Research Institute (PCORI)
Currently underway and co-led by UCLA and UC Davis, this multi-institutional clinical trial will evaluate whether Transpara can help support mammogram accuracy and patient experience in the USA. In addition to analyzing cancer detection and recall rates, the study will include focus groups and surveys to capture how patients and radiologists perceive and trust AI-assisted care.
AIMS - Norway
Want to learn more? Explore the Transpara® Breast AI Suite
Transpara® Detection
The most validated Breast AI tool, Transpara Detection helps your radiologists find more cancer and enhances their reading workflow.
Transpara® Density
Transpara Density combines a BI-RADS-like assessment as well as volumetric breast density for consistency in analysis and reporting.
Temporal Comparison
The power of priors in action: track findings across up to three prior mammograms (if available), from 9 months to 6.5 years prior.
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