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Clinical Trials/NCT03857932
NCT03857932
Recruiting
Not Applicable

Clinical Study on Regularity of Lymphatic Drainage and Surgical Treatment of Breast Cancer

Shandong University1 site in 1 country500 target enrollmentJanuary 1, 2016
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Shandong University
Enrollment
500
Locations
1
Primary Endpoint
Disease free survival
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

The investigatorsconduct the precise sentinel lymph node biopsy using preoperative computed tomographic lymphography in breast cancer. The investigators aimed to summarize the law of lymphatic drainage of breast, and to conduct the accurate surgical treatment of breast cancer.

Detailed Description

AIM:Sentinel lymph node biopsy (SLNB) is the standard technique for patients with early stage breast cancer. The investigators conduct the precise sentinel lymph node biopsy using preoperative computed tomographic lymphography in breast cancer. And The investigators identify the true sentinel lymph nodes(SLNs) followed by lymphatic ducts during operation. The investigators aimed to identify the non-sentinel lymph node, and to investigate the relationship between upper extremity lymphatic drainage. The SLNB procedure could avoid unnecessary lymph node resection and reduce treatment-related sequela. Arm1: 1. Participants received preoperative computed tomographic lymphography 2. Participants received sentinel lymph node biopsy(SLNB) 3. Participants received stained non-sentinel lymph node resection during SLNB 4. Participants received axillary reverse mapping dissection Arm2: Participants receive sentinel lymph node biopsy

Registry
clinicaltrials.gov
Start Date
January 1, 2016
End Date
December 31, 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Shandong University
Responsible Party
Principal Investigator
Principal Investigator

Qifeng Yang

Professor

Shandong University

Eligibility Criteria

Inclusion Criteria

  • histologically confirmed primary breast cancer by core needle biopsy or excisional biopsy
  • abnormal para-sentinel lymph node was found by ultrasound examination
  • ultrasound-guided fine needle aspiration cytology of these nodes were performed
  • the result of fine needle aspiration cytology was negative (no tumour cell was found)
  • participants planed to perform SLNB

Exclusion Criteria

  • pathological diagnosed ductal carcinoma in situ by excisional biopsy
  • the result of fine needle aspiration cytology was positive
  • participants has received neo-adjuvant system therapy

Outcomes

Primary Outcomes

Disease free survival

Time Frame: Up to 10 years

Time from randomization to recurrence, metastasis, appearance of a second primary tumor, or death from any cause, whichever occurs first, assessed up to 10 years.

Secondary Outcomes

  • Overall survival(Up to 10 years)

Study Sites (1)

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