Breast Cancer Clinical Trial

Study of iBreast, a Handheld Device to Detect Breast Abnormalities During Screening Visits for Breast Cancer

Summary

This study will test the iBreastExam device to find out whether it can detect a mass or lump in the breast as accurately as a routine breast cancer screening examination.

The iBreastExam is a handheld device that performs a painless electronic palpation (examination by touch) of the breast. The device is designed to detect breast abnormalities that may require breast imaging and additional clinical examination by a nurse or doctor. The iBreastExam device creates a color map of the breast, with red spots indicating areas that may be abnormal.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Female patient
Over 18 years of age, able to consent
RLC patients presenting to RLC or BAIC for mammogram and CBE
Asymptomatic and symptomatic patients will be included

Exclusion Criteria:

Male patients
Patients under 18 years of age, unable to consent
Pregnant patients
Lactating patients
Non-intact skin

Study is for people with:

Breast Cancer

Estimated Enrollment:

310

Study ID:

NCT04761055

Recruitment Status:

Active, not recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 2 Locations for this study

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MSK at Ralph Lauren (All Protocol Activities)
New York New York, 10035, United States
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York New York, 10065, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

310

Study ID:

NCT04761055

Recruitment Status:

Active, not recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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