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临床试验/NCT03715959
NCT03715959已完成不适用

Phi29 Motor Nanopore for Single Molecule Sensing: Breast Nipple Aspirate Fluid

Ohio State University Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2020年12月10日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
2
试验地点
2
主要终点
Biomarkers expression levels

研究概览

简要总结

This trial studies nipple aspirate fluid in detecting breast cancer. Nipple aspirate fluid may better detect breast cancer earlier than current methods used for screening such as mammograms and breast examinations.

详细描述

PRIMARY OBJECTIVES:

I. To obtain nipple aspirate fluid (NAF) samples from non-lactating women subjects at least 40-years-old.

II. To analyze the samples using a novel protein nanopore-based detection platform to evaluate the efficacy of the platform for breast cancer diagnosis through detection of biomarkers.

OUTLINE:

Participants and healthy volunteers undergo collection of nipple aspirate fluid from both breasts.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • BREAST CANCER: Must be > 1 year from pregnancy, lactation.
  • BREAST CANCER: Must be currently diagnosed with known breast cancer in breast.
  • BREAST CANCER: Must not be currently diagnosed with cancers other than breast cancer.
  • BREAST CANCER: Must not have been gone through surgery, radiotherapy or chemotherapy within 30 days of enrollment.
  • HEALTHY SUBJECTS: No history of breast cancer and must not be currently diagnosed with any other cancer.
  • HEALTHY SUBJECTS: Must be > 1 year from pregnancy, lactation.
  • HEALTHY SUBJECTS: Must be willing to have a clinical breast exam and/or mammogram performed or reviewed by an Ohio State University (OSU) radiologist at the James Cancer Hospital within the past 90 days prior to their NAF procedure. The clinical breast exam result and/or mammograms must be read as not suspicious for breast cancer.
  • HEALTHY SUBJECTS: Must be willing to keep the clinic informed of their breast health status for 1 year.

排除标准

  • Subjects who are currently pregnant, lactating, or within a year of pregnancy/lactation. Pregnancy testing will not be required of any patients over 60 years of age, or any patient who has undergone bilateral oophorectomy.
  • Subjects who currently are diagnosed with cancers other than breast cancer.
  • Subjects who cannot give an informed consent.
  • Male gender of any age.

结局指标

主要结局

Biomarkers expression levels

时间窗: Up to 1 year

Nipple aspiration fluid samples will be compared between breast cancer participants and healthy participants. will perform the logistic regression model for each biomarker that shows any difference between the breast cancer patients and healthy individuals. Then we will include multiple biomarkers in one model while controlling for confounders.

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

William Carson

Principal Investigator

Ohio State University Comprehensive Cancer Center

研究点 (2)

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