Clinical Trial

Cellular-Level Fluorescence Imaging for Intraoperative Margin Assessment in Breast Cancer

Study acronym: FLASH
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
Accurate intraoperative margin assessment in breast cancer surgery remains challenging. Current reliance on frozen section pathology is limited by prolonged processing time, sampling constraints, and resource intensity, contributing to variable outcomes. The EndoSCell Scanner is a novel cellular-resolution fluorescence-guided imaging technology designed to address these limitations. It enables real-time, pathology-level visualization of malignant cellular features at the surgical bed. With a 3mm probe allowing comprehensive 360° margin assessment, it reduces procedural time to under five minutes and may significantly lower secondary surgery rates. This prospective, self-controlled study aims to evaluate the accuracy of the EndoSCell Scanner for intraoperative margin assessment in patients undergoing mastectomy. Its performance will be systematically compared against both frozen section and final paraffin pathology to validate sensitivity and operational efficiency. If proven effective, this technology could become a standard adjunct tool, standardizing precision in breast cancer surgery and improving patient outcomes by enhancing surgical consistency.
Trial Details
NCT Number NCT07311317
Lead Sponsor West China Hospital
Collaborators: Fourth People's Hospital of Sichuan Province
Conditions Breast Cancer Early Stage Breast Cancer (Stage 1-3)
Enrollment 165 participants
Start Date 2026-01
Primary Completion 2027-01 (estimated)
Study Completion 2027-01 (estimated)
Updated on ClinicalTrials.gov 2025-12-30