jRCTs051210034招募中不适用
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
未提供0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Single Arm Study
- 干预模型
- Single Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 20age old over 至 90age old not(—)
- 性别
- Female
入选标准
- •(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
排除标准
- •(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
结局指标
主要结局
-
Ratio of patients who have spared axillary lymph node dissection
次要结局
未报告次要终点
研究者
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