Prospective, multicenter, randomized, controlled trial evaluating the safety and effectiveness of an absorbable antibacterial matrix device in two stage prepectoral alloplastic breast reconstruction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
702
Soft tissue support coated with antibiotics
Stanford University
Palo Alto, California, United States
RECRUITINGUniversity of Michigan Health
Ann Arbor, Michigan, United States
RECRUITINGComplications of Breast Reconstruction
Key local complications
Time frame: 6 months
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Mayo Clinic
Rochester, Minnesota, United States
Northwell Health
Staten Island, New York, United States
RECRUITINGThe Ohio State University
Columbus, Ohio, United States
RECRUITINGUPMC
Pittsburgh, Pennsylvania, United States
RECRUITINGMedical University of South Carolina
Charleston, South Carolina, United States
RECRUITINGMonument Health
Rapid City, South Dakota, United States
RECRUITINGMD Anderson Cancer Center
Houston, Texas, United States
RECRUITINGUniversity of Utah
Salt Lake City, Utah, United States
RECRUITING