Prospective, multi-center, single-arm clinical study in females undergoing immediate implant-based breast reconstruction using a pre-pectoral technique
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
259
Acellular Dermal Matrix
Historical Control Arm
Jonathan Heistein, MD Plastic & Reconstructive Surgery
Fort Worth, Texas, United States
RECRUITINGFrequency of major complication
Complications that require additional hospitalization or reoperation
Time frame: 12 months
Frequency of reconstructive failure
Removal/explantation of the breast implant
Time frame: 12 months
Change in patient reported outcomes
Change from baseline in patient reported outcomes as measured by the BREAST-Q (Scoring 0-100; 0=less satisfaction; 100= greater satisfaction)
Time frame: 12 months
Pain
Pain scores as measured by the Numerical Pain Rating Scale (NPRS) (Scoring 0-10; 0=no pain; 10= worst imaginable pain)
Time frame: 12 months
Adverse events
Reported adverse events
Time frame: 12 months
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