Breath Test to Predict Breast Cancer and Outcome of Mammography
Data Collection
Collected at a single point in time - Cross-sectionalBreast Diseases+3
+ Breast Neoplasms
+ Neoplasms
Other
Utilizing specific methods not covered by standard models in order to address unique research questions.Summary
Study start date: March 1, 2021
Actual date on which the first participant was enrolled.We will determine the accuracy of volatile organic compounds (VOCs) in the breath as predictors of risk of breast cancer and an abnormal mammogram. Breath samples will be collected using an ultra-clean collection bag and analyzed with gas chromatography surface acoustic wave detection (GC SAW) The study will be performed in two phases: Phase 1: Model-building phase (cross-sectional study): Breath VOCs will be employed to construct multivariate algorithms that distinguish between normal women and those with breast cancer and abnormal screening mammograms. Phase 2: Model-testing phase (cross-sectional study): The predictive accuracy of these algorithms will be tested to predict outcomes in normal women and those with breast cancer and abnormal screening mammograms.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.1000 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Conditions
Pathology
Criteria
Group 1: Normal screening mammogram Inclusion Criteria: 1. Female aged 18 years or older 2. Understands the study, and is willing to give written informed consent to participate 3. If a screening mammogram was performed during the preceding six month period, then the results were reported as normal (BIRADS 1 or 2) 4. If a screening mammogram was not performed during the preceding six month period, then approves collection of the results of a screening mammogram if and when it is performed subsequently\*. 5. Approves collection of relevant additional data for clinical research record if and when these data become available, including results of imaging studies, breast biopsy, and other relevant biomarker data e.g. status of BRCA1, BRCA2, HER2 and receptors (ER+ or ER-) and progesterone (PgR+ or PgR-) \* If a subsequent screening mammogram is reported as abnormal, the subject will be transferred to Group 2 for analysis of data. Exclusion Criteria: 1. Previous history of an abnormal mammogram, breast disease, or breast biopsy 2. Previous history of cancer of any site, with the exception of basal cell carcinoma of skin 3. Concurrent serious or potentially life-threatening disease (e.g. severe cardiac or infectious disease) 4. Concurrent acute pulmonary disease (e.g. influenza, influenza-like illness, acute asthma, or pneumonitis). 5. General anesthesia during the 10-day period prior to breath collection. Group 2: Abnormal screening mammogram Inclusion Criteria: Female aged 18 years or older 1. Understands the study, and is willing to give written informed consent to participate 2. Abnormal screening mammogram during preceding six months (BIRADS 3-6) 3. Approves collection of relevant additional data for clinical research record if and when it becomes available, including results of imaging studies, biopsy results, and other relevant biomarker data e.g. status of BRCA1, BRCA2, HER2 and receptors (ER+ or ER-) and progesterone (PgR+ or PgR-) Exclusion criteria: 1. Previous history of cancer of any site, with the exception of basal cell carcinoma of skin 2. Previous history of breast biopsy 3. Concurrent serious or potentially life-threatening disease (e.g. severe cardiac or infectious disease) 4. Concurrent acute pulmonary disease (e.g. influenza, influenza-like illness, acute asthma, or pneumonitis). 5. General anesthesia during the 10-day period prior to breath collection. -
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 3 locations
Zuyderland Medical Center
Heerlen, NetherlandsFrimley Health NHS Foundation Trust
Middlesex, United Kingdom