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Clinical Trial Summary

The purpose of this post-marketing study is to provide prospective evidence that the Magseed and Sentimag® is effective for lesion localization in patients undergoing surgical excision of a breast lesion and to summarize measures of product safety and performance.


Clinical Trial Description

This is a post-market, prospective, open label, single arm study of Magseed and Sentimag in patients undergoing surgical excision of a breast lesion. Subjects will have the Magseed marker deployed under imaging guidance up to thirty days prior to surgery. The Magseed marker will be localized using the Sentimag system during surgery and removed with the lesion. After the lumpectomy procedure, subjects will be evaluated for safety and patient reported outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03020888
Study type Interventional
Source Endomagnetics Inc
Contact
Status Completed
Phase N/A
Start date January 2017
Completion date July 2018

See also
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