Breast Cancer Clinical Trial

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Automated Method for Breast Cancer Detection

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Summary

Participants with suspicious breast lesions by mammography will undergo fine needle aspiration (FNA) under ultrasound guidance. The FNA will be read by the cytopathologist and analyzed in the breast cancer detection cartridge. All patients will receive standard of care (Ultrasound-guided core needle biopsy and diagnosis). We will also receive FNA collected from 60 patients with palpable lesions in South Africa and analyze them samples in our lab with the same method.

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Eligibility Criteria

Inclusion Criteria:

Patient must be female
Patient must be 18 years of age or older
Patient has been recommended for ultrasound core needle biopsy of a suspicious breast lesion

Exclusion Criteria:

Patients may be excluded for any condition that in the opinion of the investigator may not make it safe to take part (e.g. certain medicines).

Study is for people with:

Breast Cancer

Estimated Enrollment:

116

Study ID:

NCT03863522

Recruitment Status:

Terminated

Sponsor:

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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There are 2 Locations for this study

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Johns Hopkins Hospital Outpatient Center
Baltimore Maryland, 21287, United States
Johns Hopkins Medical Imaging at Green spring Station
Lutherville-Timonium Maryland, 21093, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

116

Study ID:

NCT03863522

Recruitment Status:

Terminated

Sponsor:


Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

How clear is this clinincal trial information?

Clinical Trial Resources

SurvivorNet’s Guide To Clinical Trials: What Are They And Are They Right for You?
Clinical Trials for Breast Cancer
Have You Been Diagnosed With Late-Stage Breast Cancer? Know That You Have Treatment Options.
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