About this trial
Aim of this trial is to verify whether the patients' quality of life can be improved by a less invasive surgical procedure and whether the use of robotic technique for nipple-sparing mastectomy associated to prepectoral direct implant procedure can impact on perioperative and postoperative period and on oncologic outcome.
Eligibility criteria
Qualifiers
Candidates to nipple-sparing mastectomy and immediate breast reconstruction for invasive breast cancer, ductal carcinoma in situ (DCIS), BReast CAncer gene (BRCA) mutation carriers
Any age
Negative preoperative assessment of nipple-areola complex
Absence of skin involvement
Disqualifiers
Previous thoracic radiation therapy for any reason
Inflammatory Breast Cancer
Pregnancy
Patients with psychiatric, addictive, or any disorder, which compromises ability to give informed consent for participation in this study.
Trial design
Treatments tested in this trial
- Robotic Nipple-Sparing Mastectomy