Robotic vs. Open NSM for Early Stage Breast Cancer
- Conditions
- Breast CancerBreast Cancer, Early-OnsetBreastBreast Cancer FemaleBreast Disease
- Registration Number
- NCT05720039
- Lead Sponsor
- Intuitive Surgical
- Brief Summary
This study evaluates the safety and effectiveness of the da Vinci SP Surgical System compared to Open NSM in Nipple Sparing Mastectomy procedures.
- Detailed Description
This study is a prospective, two-arm, multi-center, randomized controlled clinical investigation between RSNM and open NSM.
This study evaluates the safety and effectiveness of the da Vinci SP Surgical System compared to Open NSM in Nipple Sparing Mastectomy procedures.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 204
- Female age 21 or older
- BMI < 30
- Candidate for an NSM procedure with immediate reconstruction
- Diagnosis of early stage brest cancer
- Breast ptosis ≤ Grade 2.
- Cup size ≤ C.
- Previous breast surgery
- Diagnosis of metastatic breast cancer
- Prior radiation treatment to the chest
- Current smokers
- Contraindication for general anesthesia or surgery.
- Known bleeding or clotting disorder.
- Pregnant or suspected to be pregnant, or actively breastfeeding
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Safety: Adverse event rates Up to 42 days post-operatively Incidence of intraoperative and post-operative procedure and device-related adverse events compared to open NSM
Conversion rate Assessed during procedure Conversion is defined as conversion of da Vinci Xi robotic-assisted surgery to open surgery
Safety: positive surgical margin rates Up to 42 days post-operatively Incidence of positive surgical margins compared to open NSM
- Secondary Outcome Measures
Name Time Method Patient-Report Outcomes (BREAST-Q) Up to 5 years BREAST-Q
Oncological Outcomes (for cancer recurrence) Up to 5 years Recurrence
Oncological Outcomes (for disease-free survival) Up to 5 years Disease-free survival
Oncological Outcomes (for overall survival) Up to 5 years Overall survival
Patient-Report Outcomes (NAC Questionnaire) Up to 5 years NAC Questionnaire
Patient-Report Outcomes (EQ-5D) Up to 1 year EQ-5D
Trial Locations
- Locations (15)
City of Hope
🇺🇸Irvine, California, United States
Cedars-Sinai
🇺🇸Los Angeles, California, United States
Mayo Clinic Florida
🇺🇸Jacksonville, Florida, United States
Emory University
🇺🇸Atlanta, Georgia, United States
Endeavor Health
🇺🇸Evanston, Illinois, United States
Corewell
🇺🇸Detroit, Michigan, United States
Mayo Clinic Rochester
🇺🇸Rochester, Minnesota, United States
Washington University, St. Louis
🇺🇸St. Louis, Missouri, United States
Northwell Health
🇺🇸Lake Success, New York, United States
Duke University
🇺🇸Durham, North Carolina, United States
Scroll for more (5 remaining)City of Hope🇺🇸Irvine, California, United StatesJenny SanchezContact949-671-4057jesanchez@coh.orgStephanie Casal, MS, RN, CNSContact949-671-4112scasal@coh.orgJennifer Tseng, MDContactJamie Rand, MDContactMouchammed Agko, MDContactAntoine Carre, MDContactKatharine Schulz-Costello, DOContact