Actively Recruiting

Age: 18Years - 75Years
FEMALE
NCT07154563

Rapid Assessment of Sentinel Lymph Node Metastasis Status Using a Pan-CK-targeting NIR-II Fluorescent Probe in Breast Cancer

Led by Yunnan Cancer Hospital · Updated on 2025-09-04

60

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

Sponsors

Y

Yunnan Cancer Hospital

Lead Sponsor

X

Xiang'an Hospital of Xiamen University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Breast malignant tumors are a serious threat to women's health, and the current treatment for breast malignant tumors is still dominated by surgery, but the problems faced by patients after surgery such as edema and tumor recurrence are still relatively common, and the high recurrence rate and the occurrence of postoperative complications are closely related to the removal of metastatic lymph nodes during surgery. Therefore, accurate assessment of sentinel lymph node (SLN) metastases is essential to determine the extent of axillary lymph node dissection (ALND) and minimize complications. In this study, we developed a new technique that can rapidly distinguish between metastatic lymph nodes and normal sentinel lymph nodes (SLNs) in breast cancer patients. Briefly, fresh tissue is incubated with the probe and imaged immediately after intraoperative sentinel lymph node resection to identify the metastatic status of SLN. The accuracy of fluorescence imaging is confirmed by pathological diagnosis.

CONDITIONS

Official Title

Rapid Assessment of Sentinel Lymph Node Metastasis Status Using a Pan-CK-targeting NIR-II Fluorescent Probe in Breast Cancer

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 75 years
  • Presence of a breast nodule or mass considered resectable before surgery
  • Diagnosed with breast cancer and scheduled for sentinel lymph node biopsy or axillary lymph node dissection
  • Suitable candidate for surgery
  • Able to give informed consent and participate in the consent process
Not Eligible

You will not qualify if you...

  • Unable to participate in the consent process
  • Contraindications to surgery such as serious heart or lung disease or bleeding problems

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Yunnan Cancer Hospital, Kunming, Yunnan 650118

Kunming, Yunnan, China

Actively Recruiting

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Research Team

J

Junhong Chen, Postgraduate

CONTACT

W

Weiling Chen, Doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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