Actively Recruiting
Identifying Patterns in the Breath of Individuals With Breast Cancer
Led by Breathe BioMedical Inc · Updated on 2026-04-22
5175
Participants Needed
4
Research Sites
144 weeks
Total Duration
On this page
Sponsors
B
Breathe BioMedical Inc
Lead Sponsor
M
Mayo Clinic
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers will compare the breath profiles of women with breast cancer and those without to determine whether there are disease-specific patterns that can be leveraged to facilitate breast cancer detection. Women with mammogram-confirmed breast tissue density undergoing standard-of-care breast cancer screening will be invited to participate. Those who provide informed consent will provide one breath sample and fill out a questionnaire about their medical history with help from the research coordinators. Breath samples will be collected prior to standard of care biopsy or MRI, and patients will be stratified into the case or control group based on their test results. The primary goal of this project is to use exhaled alveolar breath and the subsequent spectral data produced by Breathe BioMedical's cavity ring-down spectrometer to further develop Breathe BioMedical's technology and machine learning algorithms to determine the feasibility of detecting breast cancer in women aged 40 to 74. Secondarily, this project aims to identify patterns of VOCs that are either over- or under-represented in participants with breast cancer when compared to the breath profiles of participants without breast cancer. This project will also assess performance characteristics of the technology (e.g. sensitivity, specificity, false negative rate, and false positive rate) including subgroup analyses. This project aims to understand intra-subject variability by exploring differences in breath signatures before and after definitive management of breast cancer, including surgical resection.
CONDITIONS
Official Title
Identifying Patterns in the Breath of Individuals With Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female (sex as assigned at birth)
- Aged 40 to 74 years
- Mammography confirmed breast tissue density (BI-RADS density score of A, B, C, or D)
- Scheduled for standard of care biopsy or MRI
- Fluent in English, Spanish, or French
- Able to give informed consent
- Able to provide a breath sample
You will not qualify if you...
- Prior history of breast cancer
- Surgical biopsy or surgical excision of breast cancer in the past six months
- History of cancer (except basal cell or squamous cell carcinoma of the skin) in the past year
- Acute respiratory infection or symptoms in the past seven days
- MRI BI-RADS 3 undergoing active surveillance requiring six-month follow-up
- Pregnant or become pregnant during the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
GW Comprehensive Breast Center
Washington D.C., District of Columbia, United States, 20037
Actively Recruiting
2
Mayo Clinic Breast Clinic
Jacksonville, Florida, United States, 32224
Actively Recruiting
3
Duke University Medical Cente
Durham, North Carolina, United States, 27710
Actively Recruiting
4
Weinstein Imaging Associates
Pittsburgh, Pennsylvania, United States, 15220
Not Yet Recruiting
Research Team
S
Sandra Veenstra
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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