Single port endoscopic surgery for early breast cancer
Prospective Clinical Study of Single Port Endoscopic Breast Conserving Surgery or Open Breast Conserving Surgery for Early Breast Cancer
This study is testing if a new type of minimally invasive breast surgery can help women with early-stage breast cancer recover better and have better cosmetic results compared to traditional surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 20 Years to 70 Years |
| Sex | Female |
| Sponsor | First Affiliated Hospital Xi'an Jiaotong University Academic / other |
| Locations | 1 site (Xi'an, Shaanxi) |
| Trial ID | NCT06593132 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of single port endoscopic breast conserving surgery (E-BCS) compared to traditional open breast conserving surgery (C-BCS) for patients with early-stage breast cancer. It aims to gather high-level evidence to support the development of endoscopic techniques in breast cancer treatment. The study will analyze surgical outcomes, cosmetic results, and patient recovery to determine the advantages and disadvantages of both surgical approaches.
Who should consider this trial
Good fit: Ideal candidates are female patients aged 20 to 70 with early-stage breast cancer (tumor size <5 cm, TNM stage 0-II).
Not a fit: Patients with bilateral breast cancer or those requiring reconstruction after breast conserving surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to less invasive surgery with improved cosmetic outcomes for patients with early breast cancer.
How similar studies have performed: While there is ongoing interest in endoscopic techniques, this specific approach is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Breast cancer confirmed by pathology； 2. Tumor \<5 cm, TNM stage 0-II； 3. Single Port Endoscopic or traditional open surgery; (4)20 to 70 years old female patients. Exclusion Criteria: 1. Bilateral breast cancer; 2. Reconstruction after breast conserving surgery ; 3. Basic information is not complete； 4. Breast conserving surgery was converted to modified radical resection or subcutaneous adenoidectomy.
Where this trial is running
Xi'an, Shaanxi
- the First Affiliated Hospital of Xi'an Jiaotong University — Xi'an, Shaanxi, China (Recruiting)
Study contacts
- Study coordinator: Zhaoli Nan, bacheior
- Email: 369075227@qq.com
- Phone: 15114822852
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.