Safety and Feasibility of Robotic SP Nipple Sparing Mastectomy
Sponsor: Deborah Farr, MD • ClinicalTrials.gov ID: NCT05245812
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This is a single arm, single-center, prospective clinical trial designed to track the peri, post-operative and oncologic outcomes when utilizing the da-Vinci single port (SP) robotic platform to perform robotic nipple sparing mastectomy (rNSM) and immediate breast reconstruction with tissue expanders/implants and acellular dermal matrix (ADM - Alloderm), for patients with breast cancer as well as those with a high risk for breast cancer. Safety and feasibility measures will be measured as primary outcome measures. Oncological and patient satisfaction outcome measures will be measured. Our hypothesis is that SPr-NSM is equal to open NSM in terms of safety, feasibility and oncological outcomes with improved patient satisfaction as measured by nipple sensation and patient reported outcomes.
Interventions
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da Vinci SP Surgical System
(Device)
This is a software-controlled, electro- mechanical system designed for surgeons to perform single port minimally invasive surgery.
Eligibility criteria
Conditions
Locations
- UT Southwestern — Dallas, Texas, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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