← Eichor
Study identifier: NCT07222514 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: DIEP Flap Breast Reconstruction  ·  Sponsor: Vanderbilt University Medical Center

PhaseNA
Planned participants4
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Emmanuel Giannas, MD  ·  6154033398  ·  e.giannas@vumc.org

Jun Yao  ·  jun.yao@vumc.org

Always discuss trial participation with your own doctor first.

Locations (1)

Vanderbilt University Medical CenterNashville, Tennessee, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07222514