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Clinical Trial Summary

This is a prospective, open-label, within-patient clinical trial to determine the accuracy of Indocyanine green (ICG) guided sentinel lymph node biopsy (SLNB) compared to the standard dual-tracer SLNB in breast cancer patients who have had chemotherapy as a first treatment using a non-inferiority design. Patients with operable breast cancer treated with chemotherapy and eligible for SLNB will be included in the study. During surgery, ICG will be injected and used to identify fluorescent sentinel nodes using a hand-held imaging camera; radiotracer and blue dye will also be used as per standard protocols. Intraoperative and clinicopathologic outcomes such as complications, characteristics of nodes, false negative rates and feasibility will be assessed. Patients will be asked to complete standardized patient reported outcome questionnaires (Breast-Q, FACT-B+4, VAS) to define the patient experience with this novel technique.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06085274
Study type Interventional
Source University Health Network, Toronto
Contact Tulin Cil, MD MSc FRCSC
Phone 416-946-4501
Email tulin.cil@uhn.ca
Status Recruiting
Phase N/A
Start date June 1, 2024
Completion date April 30, 2026

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