Feasibility and Safety of Single-Port Robotic-Assisted Deep Inferior Epigastric Pedicle Flap Harvest

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorVanderbilt University Medical Center

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).

Eligibility criteria

Qualifiers

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.

Disqualifiers

History of prior abdominal surgery that significantly compromises perforator vessel integrity.

Pregnant woman.

Prisoners.

BMI > 35, as measured during the preoperative evaluation.

Trial design

Treatments tested in this trial

  • Single-Port Robotic System

Treatment groups

4 Participants
are divided into 1 treatment group

Sponsors and collaborators