Comparison Between Prepectoral and Subpectoral Breast Reconstruction

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-70
SponsorBeijing Friendship Hospital

About this trial

There are controversies about breast implant-based reconstruction techniques. Our center pioneered single-port insufflation endoscopic nipple-sparing mastectomy (SIE-NSM) combined with stage I prosthesis reconstruction. The study's primary objective is to compare single-port endoscopic NSM combined with pre-pectoral breast reconstruction to the subpectoral breast reconstruction group regarding breast satisfaction.

This study is an ambispective cohort study. The study will be conducted at Beijing Friendship Hospital, affiliated with Capital Medical University. Patients will be enrolled retrospectively from January 2014 to March 2022 by reviewing the medical records and recruited prospectively from March 2022 to March 2025. The two cohorts are the pre-pectoral breast reconstruction cohort and the subpectoral breast reconstruction cohort, both following single-port insufflation endoscopic nipple-sparing mastectomy. The primary outcome of this study is postoperative breast satisfaction, which the BREAST-Q score will measure. The different variables will be compared using the Χ2 test for categorical variables and the Mann-Whitney test for continuous variables.

Eligibility criteria

Qualifiers

Female patients with preoperative pathologically confirmed early-stage invasive breast cancer (stage I or stage II) by core needle biopsy.

Breast-conserving surgery is not possible due to the presence of contraindications to breast-conserving surgery, or the patient actively requests total mastectomy.

Patients having willingness for breast reconstruction.

Age between 18 to 70 years.

Disqualifiers

patients having serious medical diseases, including unstable angina pectoris, myocardial infarction, and cerebrovascular accident within 6 months.

Having history of malignant tumor (s) within 5 years.

Patients under immunosuppressive therapy for organ transplantation.

Having continuous systemic steroid hormone therapy.

Trial design

Treatments tested in this trial

  • The breast reconstruction method after single-port insufflation endoscopic nipple-sparing mastectomy

Treatment groups

88 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Beijing Friendship Hospital

Lead sponsor

Beijing Health Promotion Association

Collaborator