Expired Study
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Saint Louis, Missouri 63110


Purpose:

The investigators propose a randomized controlled superiority trial of standard breast-conserving surgery (BCS) versus BCS with cavity shave margins (CSM). The main objectives of this trial will be to evaluate prospectively the impact of routine standardized CSM on margin status following primary surgery for early stage breast cancer (Stage 0 - II), on post-operative patient satisfaction and cosmetic outcomes, and on general intraoperative time and operative costs. A parallel group format will be implemented to compare this modified surgical therapy - BCS with CSM - with BCS alone, which is the current standard of care.


Criteria:

Inclusion Criteria: - Newly diagnosed, biopsy-proven stage 0-II breast cancer. - Planning to undergo breast-conserving surgery. - At least 18 years of age and no more than 85 years of age. - Female. - Able to understand and willing to sign an IRB-approved written informed consent document. Exclusion Criteria: - Prior surgical treatment for this diagnosis. - Undergone neoadjuvant chemotherapy. - History of prior chest radiation therapy. - Known metastatic disease. - Pregnant. - Preference for mastectomy instead of breast-conserving surgery. - History of ipsilateral breast cancer. - Goggle assessment substudy: Iodine or seafood allergies.


NCT ID:

NCT02462200


Primary Contact:

Principal Investigator
Julie Margenthaler, M.D.
Washington University School of Medicine


Backup Contact:

N/A


Location Contact:

Saint Louis, Missouri 63110
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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