A Novel Fluorescent Ductal Needle for Localization and Sampling of High-risk Breast Micro Lesions

Recruiting Observational Study
Mammary Tumor Nipple Discharge
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 75
Sex
Female
Study type
Observational
Participants needed
300 (estimated)
Sponsor
The Fourth Affiliated Hospital of China Medical University · Other
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About This Trial
This retrospective cohort study investigates the differences in the reliability of rapid pathology compared to postoperative pathology when utilizing a novel fluorescent localization needle equipped with a controllable shedding quantum dot chiral nanofluorescent coating, in contrast to traditional localization techniques for breast duct lesions. The primary goal is to evaluate the clinical effecti…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Female patients aged 18-75 years. 2. Patients who have been diagnosed intraductal breast lesion by ductoscopy. 3. Patients who have undergone ductal excision. Exclusion Criteria: 1. Pregnant or breastfeeding. 2. Patients who have known allergy to quantum-dot materials or lo…
Contacts

Jian Wen, MD

+86 18900912982

wenjian@cmu.edu.cn

CONTACT