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Robotic Surgery
Robotic vs. Open Mastectomy for Breast Cancer (SP NSM Trial)
N/A
Recruiting
Research Sponsored by Intuitive Surgical
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Breast ptosis ≤ Grade 2
Diagnosis of early stage breast cancer
Must not have
Contraindication for general anesthesia or surgery
Previous breast surgery
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial compares the safety and effectiveness of a new robotic surgery tool, the da Vinci SP Surgical System, to traditional open surgery for patients undergoing breast surgery that spares the nipple. The robotic system aims to improve precision and recovery. The da Vinci SP Surgical System is one of the latest versions of robotic surgery systems, designed for minimally invasive procedures.
Who is the study for?
This trial is for women over 21 with a breast cup size of C or smaller, BMI under 30, diagnosed with early stage breast cancer and suitable for Nipple Sparing Mastectomy (NSM) with immediate reconstruction. It's not for those who've had previous breast surgery, are pregnant/breastfeeding, have bleeding/clotting disorders, prior chest radiation treatment, smoke currently or can't undergo general anesthesia.
What is being tested?
The study compares the safety and effectiveness of two types of mastectomy procedures: one using the da Vinci SP Surgical System (Robotic NSM) and the other traditional open surgery (Open NSM). The goal is to see which method might be better for patients undergoing nipple sparing mastectomies.
What are the potential side effects?
While specific side effects aren't listed here, typical risks may include pain at the surgical site, infection risk from incisions, potential complications from anesthesia and possible differences in recovery time between robotic versus open surgery.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My breast sagging is mild to moderate.
Select...
I have been diagnosed with early stage breast cancer.
Select...
I am a woman aged 21 or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot have general anesthesia or surgery due to health risks.
Select...
I have had breast surgery before.
Select...
I have a known bleeding or clotting disorder.
Select...
I have had radiation treatment to my chest before.
Select...
My breast cancer has spread to other parts of my body.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Conversion rate
Safety: Adverse event rates
Safety: positive surgical margin rates
Secondary study objectives
Oncological Outcomes (for cancer recurrence)
Oncological Outcomes (for disease-free survival)
Oncological Outcomes (for overall survival)
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Robotic NSM with da Vinci SPExperimental Treatment1 Intervention
Subjects randomized to this arm will undergo robotic NSM (RNSM) procedures
Group II: Open NSMActive Control1 Intervention
Subjects randomized to this arm will undergo conventional open NSM procedures
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for breast disease, particularly breast cancer, include surgical options such as mastectomy and lumpectomy, often combined with radiation therapy, chemotherapy, and hormone therapy. Robotic-assisted surgery, like the da Vinci SP Surgical System, enhances precision in procedures such as nipple-sparing mastectomy (NSM) by providing better visualization and dexterity.
This minimally invasive approach reduces recovery time and surgical complications. Understanding these mechanisms is crucial for patients as it helps them make informed decisions about their treatment options, balancing efficacy with quality of life considerations.
Local Breast Cancer Recurrence after Mastectomy and Breast-Conserving Surgery for Paget's Disease: A Meta-Analysis.
Local Breast Cancer Recurrence after Mastectomy and Breast-Conserving Surgery for Paget's Disease: A Meta-Analysis.
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Who is running the clinical trial?
Intuitive SurgicalLead Sponsor
77 Previous Clinical Trials
50,357 Total Patients Enrolled
Madhu GorrepatiStudy DirectorIntuitive
Kathryn WineStudy DirectorIntuitive Surgical
1 Previous Clinical Trials
60 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot have general anesthesia or surgery due to health risks.My breast sagging is mild to moderate.I have been diagnosed with early stage breast cancer.You have a cup size smaller than C.I have had breast surgery before.I am a woman aged 21 or older.I am eligible for nipple-sparing mastectomy with immediate reconstruction.You weigh less than 30% more than what is considered healthy for your height.I have a known bleeding or clotting disorder.I have had radiation treatment to my chest before.You are currently smoking cigarettes.My breast cancer has spread to other parts of my body.
Research Study Groups:
This trial has the following groups:- Group 1: Robotic NSM with da Vinci SP
- Group 2: Open NSM
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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