Feasibility and Safety of Single-Port Robotic-Assisted Deep Inferior Epigastric Pedicle Flap Harvest
Recruiting
N/A
Interventional Study
DIEP Flap Breast Reconstruction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Device Feasibility
- Participants needed
- 4 (estimated)
- Sponsor
- Vanderbilt University Medical Center · Other
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About This Trial
The primary aim of this study is to evaluate the feasibility of single-port robotic surgery for DIEP flap breast reconstruction. The investigators will also investigate complications of the procedure, incision length, flap success rate, post operative pain, vascular pedicle length and caliber, and VMP-B score (quality of life/satisfaction of breast procedures survey).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female patients aged ≥18 years.
* Candidates for unilateral or bilateral breast reconstruction using a DIEP flap.
* No contraindications for general anesthesia or robotic surgery.
* Patients with adequate abdominal donor tissue for DIEP flap harvest.
Exclusion Criteria:
* Hi…
Contacts