Efficacy and Accuracy of Combined Localization Versus Single Localization in Non-palpable Breast Cancer: a Prospective Randomized Control Trial.

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The standard method for localizing non-palpable breast cancer is currently preoperative wire-guided localization, its positive margin rate still remains around 20-50%. This study aims to compare the accuracy and efficacy of wire vs. combined breast tissue markers in localizing non-palpable breast cancer.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• female patients, age≥18 year

• A score of ≥ 2 on the Eastern Cooperative Oncology Group scale

• Patients pathologically diagnosed with untreated breast cancer by core-needle biopsy, with histologically confirmed non-palpable in situ cancer, including pleomorphic lobular carcinoma in situ or invasive non-palpable breast cancer that required localization

• Patients are willing to undergo breast conserving surgery and have no contraindications to breast conserving surgery.

Locations
Other Locations
China
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
RECRUITING
Guangzhou
Contact Information
Primary
Chang Gong, doctor
changgong282@163.com
02034070499
Time Frame
Start Date: 2023-02-17
Estimated Completion Date: 2025-12-01
Participants
Target number of participants: 170
Treatments
Experimental: Untreated patients-combined localization
In untreated non-palpable breast cancer patients, positioning focus use wire and marker clip at 1day before operation
Active_comparator: Untreated patients-single localization
In untreated non-palpable breast cancer patients, positioning focus use wire at 1day before operation
Related Therapeutic Areas
Sponsors
Leads: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

This content was sourced from clinicaltrials.gov