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Trial Title:
Application of Rapid On-site Evaluation in Lymph Node Biopsy of Breast Cancer
NCT ID:
NCT06495736
Condition:
Breast Cancer
Conditions: Official terms:
Breast Neoplasms
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
Non-Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Diagnostic
Masking:
None (Open Label)
Intervention:
Intervention type:
Diagnostic Test
Intervention name:
Experimental: ROSE technique stain
Description:
The ROSE technical group uses Diff-Quick stain for diagnosis
Arm group label:
ROSE technique
Summary:
The goal of this clinical trial is to evaluate the value of rapid on-site
evaluation（ROSE） in lymph node biopsy of breast cancer. The main question it aims to
answer is:The ROSE technique was applied to breast cancer lymph node biopsy to improve
the diagnostic efficiency and accuracy.
Participants underwent routine lymph node biopsy, and the test personnel conducted
routine disease examination and rose technique evaluation on the removed ly
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Patients had pathologically confirmed primary breast cancer
- Surgical treatment was available
Exclusion Criteria:
- Previous history of surgery on the affected axilla, internal breast or chest
- Pregnant or breastfeeding patients
- Previous radiotherapy or chemotherapy
- Complicated history of other tumors
Gender:
Female
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Yunnan Cancer Hospital
Address:
City:
Kunming
Country:
China
Status:
Recruiting
Contact:
Last name:
Hui Li, Master's degree
Phone:
18468212816
Email:
249045140@qq.com
Start date:
February 1, 2024
Completion date:
February 2026
Lead sponsor:
Agency:
Yunnan Cancer Hospital
Agency class:
Other
Source:
Yunnan Cancer Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06495736
