Breath Test to Predict Breast Cancer and Outcome of Mammography
Colección de datos
Recopilados en un punto de tiempo - TransversalEnfermedades de la Mama+2
+ Neoplasias de la Mama
+ Neoplasias
Otro
Uso de métodos específicos que no están cubiertos por los modelos estándar para abordar preguntas de investigación únicas.Resumen
Fecha de inicio: 1 de marzo de 2021
Fecha en la que se inscribió al primer participante.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.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 1000 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Otro
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Mujer
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Condiciones
Patología
Criterios
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. -
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Objetivos del Estudio
Objetivos Primarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene 3 ubicaciones
Zuyderland Medical Center
Heerlen, NetherlandsFrimley Health NHS Foundation Trust
Middlesex, United Kingdom