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Life sciences · Interventional Study
ClinicalTrials.gov · November 6, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07029646). This is a study registration, not published results. Lead sponsor: Peking University Cancer Hospital & Institute. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 87 participants (ACTUAL). Conditions: Breast-Conserving Surgery, Breast Carcinoma, Margins in the Specimen. Interventions: DEVICE: EndoScell™ intraoperative handheld microscope. Primary outcome measures: Accuracy , Within 7 days after the operation. Brief summary: The goal of this clinical trial is to assess whether cell microscopic imaging can accurately determine the tumor-free status of surgical margins in breast cancer patients undergoing breast-conserving surgery. This study involves female patients aged 18-70 years with breast cancer who are candidates for breast-conserving surgery. The main question it aims to answer is: \- Can cell microscopic imaging provide accurate intraoperative assessment of surgical margins compared to standard frozen pathology? Researchers will compare the results of cell microscopic imaging to those of standard frozen pathology and paraffin pathology to see if the new imaging technology can effectively and quickly determine whether surgical margins are free of cancer cells. Participants will: * Undergo breast-conserving surgery with standard pathological assessments. * Have their surgical margins evaluated using cell microscopic imaging during the operation. * Be monitored for postoperative recovery at regular intervals (2 weeks, 3 months, 6 months, and 12 months) after the surgery.