Accessory Breast
Conditions
Interventions
Experimental Group:Surgery was performed with the test device
Previous clinical routine cases of accessory breast surgery combining liposuction and gland excision:None
Sponsors
Shenzhen People’s Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients who were clinically diagnosed as accessory breast by palpation, color Doppler ultrasound or magnetic resonance imaging (MRI) before surgery and willing to undergo accessory breast surgery; 2.Disease duration>=1 year, age >=18 and <=65 years old; 3.No history of common accessory breast diseases such as breast and axilla; 4.Voluntarily participated in the clinical trial and signed the informed consent.
Exclusion criteria
Exclusion criteria: 1.Abnormal coagulation function; 2. Complicated with severe liver and kidney dysfunction, local infection, malignant tumor, and other diseases intolerant to surgery; 3. Palpable nodular mass; 4. Those suffering from mental illness or unable to cooperate; 5. Pregnant women; 6. Other subjects considered by the investigator to be unsuitable for the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effect 6 months after operation (patients' satisfaction with axillary shape change, affected limb movement, and axillary skin smoothness) : BREAST surgery evaluation scale The BREAST-Q.; | — |
Secondary
| Measure | Time frame |
|---|---|
| Length of incision during operation;Duration of surgical procedure;Intraoperative blood loss;Duration of postoperative drainage tube removal;Vancouver Scar ;Patient satisfaction at 3 months after surgery (including patient satisfaction with axillary shape change, limb movement on the affected side, and axillary skin smoothness); | — |
Countries
China
Contacts
Public ContactDai Damao
Shenzhen People’s Hospital
Outcome results
None listed