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Clinical Trial Summary

Women who attend for their screening mammogram will be recalled if an abnormality is detected on the screening mammogram. Calcifications account for 20% of the women recalled to second stage screening. Currently there is no effective imaging tool to determine if the calcifications are cancer or not. Therefore, 90% of women will be subjected to a biopsy. 25-30% of the biopsies will show cancer. Contrast enhanced spectral mammography (CESM) is where contrast is given and then a mammogram performed. The theory is that high risk DCIS and invasive cancers have an increased blood supply and will therefore enhance more than benign lesions within the breast. If CESM can identify calcifications that are cancerous then we maybe able to reduce the number of women who have benign biopsies. This is patient focused as women would not require a biopsy and be able to be reassured at the same visit. This is also a cost-saving for the Trust by reducing unnecessary biopsies. This also supports the findings of the Marmot review by aiming to reduce harm by over-diagnosis.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT03857152
Study type Interventional
Source The Leeds Teaching Hospitals NHS Trust
Contact Nisha Sharma, MBChB; MRCP; FRCR; M
Phone 01132063798
Email nisha.sharma2@nhs.net
Status Recruiting
Phase N/A
Start date December 3, 2018
Completion date February 2, 2021

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