Single Port Endoscopic Breast Conserving Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: endoscopic breast conserving surgery.
- Who it may be relevant to
- Registry conditions: Breast Conserving Surgery, Endoscopic Surgery. Basic parameters: 20 years — 70 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Prospective Clinical Study of Single Port Endoscopic Breast Conserving Surgery or Open Breast Conserving Surgery for Early Breast Cancer
Overview
The center plans to carry out a prospective clinical study of single hole total endoscopic breast conserving surgery for early breast cancer compared with open breast conserving surgery, to provide high-level evidence-based medical evidence for the development of endoscopic breast conserving surgery for early breast cancer.
Detailed description
Data show that breast cancer has surpassed lung cancer asthemost prevalent malignant tumor in the world, and traditional open surgery is highly invasive and has poor cosmetic results. This study investigates the results of endoscopic breast- conserving surgery(E-BCS) versus conventional breast-conserving surgery(C-BCS) in the treatment of patients with early-stage breast cancer and to compare the advantages and disadvantages of the two surgical procedures, so as to provide the best evidence for the rational choice of the procedure by both doctors and patients.
Interventions
- Procedure endoscopic breast conserving surgery
Breast endoscopy technology completes complex surgical operations through small incisions, achieving aesthetically pleasing results while ensuring tumor safety.
Primary outcome measures
- Six months after operation SURVIVAL EFFECTS [Time frame: From enrollment to the end of 6 months after surgery]
Secondary outcome measures (3)
- Intraoperative blood loss [Time frame: From the beginning to the end of the operation]
- Postoperative drainage volume in the first three days after breast conserving surgery [Time frame: 3 days after surgery]
- Length of surgical incision [Time frame: 1 week after surgery]
Eligibility criteria
Inclusion criteria
- Breast cancer confirmed by pathology；
- Tumor <5 cm, TNM stage 0-II；
- Single Port Endoscopic or traditional open surgery; (4)20 to 70 years old female patients.
Exclusion criteria
- Bilateral breast cancer;
- Reconstruction after breast conserving surgery ;
- Basic information is not complete；
- Breast conserving surgery was converted to modified radical resection or subcutaneous adenoidectomy.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- the First Affiliated Hospital of Xi'an Jiaotong University — Xi'an
Identifiers
NCT: NCT06593132 · SPEBCS-2023