JPRN-jRCTs051210034
Recruiting
未知
Clinical Trial for the Evaluation of Efficacy and Safety of Contrast Enhanced Ultrasonography-guided Sentinel Lymph Node Biopsy after Introducing Twirl Breast Marker for Axillary Lymph Node-positive Breast Cancer
Miyake Tomohiro0 sites20 target enrollmentJune 4, 2021
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Breast cancer
- Sponsor
- Miyake Tomohiro
- Enrollment
- 20
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Patients with the ability to consent who are 20 years old or older and younger than 90 years old at the time of obtaining informed consent
- •(2\) Clinically T1\-2N1M0 breast cancer patients with 1 to 2 positive axillary lymph nodes of whicn at least one axillary lymph node has been confirmed to harbor metastasis by fine needle aspiration cytology
- •(3\) Patients whose condition are expected to be stable for longer than 6 months at the time of obtaining the informed consent
- •(4\) Patients for whom a written consent has been obtained for participation in this study
Exclusion Criteria
- •(1\) Patients with palpable hard nodes
- •(2\) Patients with radiologically proven matted nodes or gross extranodal disease
- •(3\) Patients who have been treated with preoperative chemotherapy or hormonal therapy for breast cancer
- •(4\) Patients who are during or possibilities of pregnancy
- •(5\) Patients who are allergic to metal or egg
- •(6\) Patients with coronary artery disease
- •(7\) Patients who seem not eligible for the present study
Outcomes
Primary Outcomes
Not specified
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