跳至主要内容
临床试验/NCT07339306
NCT07339306招募中不适用

A Novel Fluorescent Ductal Needle With Controllable Detachment for Realtime Localization and Sampling of Micro Lesions in Breast Ducts: a Prospective, Multicenter Study

The Fourth Affiliated Hospital of China Medical University1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2026年1月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
300
试验地点
1
主要终点
pathological assessment concordance rates

研究概览

简要总结

This prospective, multicenter 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 principal objective is to assess the clinical efficacy of this innovative fluorescent localization needle in enabling precise pathological diagnosis of micro lesions in breast ducts.

详细描述

The diameter of breast ducts is less than 0.7 mm, presenting a significant technical challenge for the precise localization of early-stage, small lesions during surgical and pathological sampling. These early microlesions typically measure only a few millimeters, necessitating surgeons to increase excision margins to minimize the risk of overlooking them. However, this approach complicates the pathologists' ability to accurately identify these microlesions during diagnosis, thereby increasing the likelihood of missed diagnoses and the potential need for additional surgical interventions. Current localization methods, including liquid methylene blue and conventional localization needles, exhibit a high rate of pathological missed diagnoses due to localization inaccuracies and specimen contamination. Consequently, there is an urgent need to develop innovative localization technologies capable of facilitating the precise identification of millimeter-scale microlesions within breast ducts. A prospective multicenter study is required to compare the consistency of intraoperative and postoperative pathological assessments between a novel fluorescent localization needle-featuring a controllable shedding quantum dot chiral nanofluorescent coating-and traditional localization techniques employed in breast duct lesion surgeries. The primary objective is to evaluate the clinical efficacy of this new fluorescent localization needle in enhancing the accuracy of pathological diagnosis of microlesions within breast ducts and to improve the precision of pathological evaluations.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients aged 18-75 years.
  • Patients scheduled to undergo duct excision surgery.
  • Patients who are capable of providing written informed consent and adhering to the study protocols.

排除标准

  • Pregnant or breastfeeding.
  • Patients who have known allergy to quantum-dot materials or localization needle components.
  • Patients with active hepatitis B or C infection with detectable viral load.
  • Patients with unstable cardiovascular disease (e.g., recent myocardial infarction, uncontrolled arrhythmia, NYHA class III-IV heart failure).
  • Patients with history of neurological or psychiatric disorders that may impair compliance (e.g., epilepsy, dementia).
  • Patients who concurrent participation in another interventional clinical trial.

研究组 & 干预措施

Conventional Localization Group

Active Comparator

Patients received breast ductal excision surgery utilizing conventional localization methods.

干预措施: conventional localization marker needle (Device)

Fluorescent Localization Group

Experimental

Patients received breast ductal excision surgery utilizing a novel fluorescent localization marker needle.

干预措施: novel fluorescent localization marker needle (Device)

结局指标

主要结局

pathological assessment concordance rates

时间窗: From enrollment to the end of treatment at 6 weeks

Evaluate and compare the discrepancies in the consistency of intraoperative frozen and postoperative paraffin-embedded pathological assessments between subjects undergoing breast duct excision surgery utilizing a novel fluorescent localization marker needle and those employing conventional localization methods.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

JIAN WEN

Director of the Ninth General Surgery Department

The Fourth Affiliated Hospital of China Medical University

研究点 (1)

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