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临床试验/KCT0002377
KCT0002377已完成未知

Intraoperative Sentinel Lymph Node Detection Using Fluorescein in Breast Cancer

Korea University Ansan Hospital0 个研究点目标入组 61 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
61

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
o Limit 至 o Limit(—)
性别
Female

入选标准

  • Patients with breast cancer who needs sentinel lymph node biopsy during operation

排除标准

  • 1. Patients who does not need sentinel lymph node biopsy because of biopsy proven metastatic lymph nodes
  • 2. Any medical condition or prior therapy that, in the opinion of the investigator, would make the subject unsuitable for this study
  • 3. Hypersensitivity to fluorescein solution
  • 4. Having a heart condition, feeling chest pain during physical activity, experiencing chest pain, becoming dizzy/ever losing
  • balance or consciousness
  • 5. Being pregnant or breastfeeding
  • 6. Having a general weakness

研究者

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