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Clinical Trials/KCT0002377
KCT0002377
Completed
未知

Intraoperative Sentinel Lymph Node Detection Using Fluorescein in Breast Cancer

Korea University Ansan Hospital0 sites61 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Korea University Ansan Hospital
Enrollment
61
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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