Improved Successful Retrieval Rate of HydroMARK Plus Breast Biopsy Site Marker in Comparison to HydroMARK as Well as Improved Surgeon Satisfaction

Recruiting N/A Interventional Study
Breast Neoplasm
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 90
Sex
Female
Study type
Interventional
Purpose
Diagnostic
Participants needed
150 (estimated)
Sponsor
University of Alabama at Birmingham · Other
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About This Trial

The purpose of the study is to test how successful the retrieval rate of the new HydroMARK Plus Breast Biopsy Site Marker in comparison to HydroMARK.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with biopsy clips scheduled for surgery with SCOUT localization Exclusion Criteria: * Patients who didn't have surgery, patients younger than 18 years old * Patients older than 90 years old * Inmates * Non-English speakers
Contacts

Quenteeria Mooney

205-996-1082

qmooney@uabmc.edu

CONTACT