Cosmetic Outcome of Electrocautery, Scalpel and PEAK PlasmaBlade for Surgical Breast Incisions
Surgical Wound Infection | Post-operative Pain | Postoperative Complications | Wound Complication | ScarThis study will compare the cosmetic scar result from the use of scalpel, electrocautery, and pulsed electron avalanche knife (PEAK) PlasmaBlade (PPB) for the initial skin incision for total mastectomy procedures without immediate breast reconstruction.
It is hypothesized that there will be no significant difference in mastectomy scar cosmesis.
The purpose and objectives of this study are:
1. To evaluate and compare the cosmetic scar result from the use of scalpel, standard electrocautery, or PEAK PlasmaBlade for initial incision for total mastectomy procedures without immediate breast reconstruction.
2. To inform future equipment choices for breast surgery including potential elimination of scalpels and their attendant risks.
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
0 and up
Critères de participation
Inclusion Criteria:
* Patients having a total mastectomy with or without axilla surgical staging
Exclusion Criteria:
* Patients having immediate breast reconstruction
* Patients with a diagnosis of inflammatory breast cancer
* History of keloid scar formation
* History of connective tissue disorder (scleroderma or rheumatoid arthritis with skin involvement)
* Patients with prior incision at the planned mastectomy site.
* Patients with known suture hypersensitivity
* Patients with evidence of current infection
Lieu de l'étude
Mount Saint Joseph Hospital
Mount Saint Joseph HospitalVancouver, British Columbia
Canada
Contactez l'équipe d'étude
Elaine C McKevitt, MD, FRCSC
Kathryn Isaac, MD, FRCSC
Melina Deban, MD, FRCSC
Rebecca Warburton, MD, FRCSC
Bennett B Westmore
Carol K Dingee, MC, FRCSC
Jieun Newman-Bremang, MD, FRCSC
Lisa Aird, MD, FRCSC
Jin-Si Pao, MD, FRCSC
Amy K Bazzarelli, MD, FRCSC
Yuwei Yang, MSc
- Étude parrainée par
- University of British Columbia
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06191159