Condition: Lung Cancer · Sponsor: bioAffinity Technologies Inc.
The primary objective of this study is to compare Assay results to diagnoses determined by currently accepted standards for lung cancer detection. This will be accomplished by analysis of sputum samples from three cohorts including healthy Participants, high risk Participants, and cancer patient Participants using the Assay as developed in accordance with findings of bioAffinity protocol BA-001 to confirm assay results. Adjustments will be made as necessary to finalize Assay design for clinical trials and commercialization. The secondary objective of this study is to determine optimum methods for collection of sputum samples. Three sputum collection methods used by high risk Participants will be compared. Individuals at high risk for lung cancer will be assigned to one of three sputum collection cohorts including (1) acapella® airway assist device under medical supervision to obtain a single sputum sample; (2) acapella® airway assist device to obtain a sputum sample over a three-day period, and (3) individuals who under medical supervision will collect a single sputum sample assisted by nebulization of between 0.9% to 10% hypertonic saline. Samples will be compared to determine the optimal collection method for sample analysis by CyPath® Lung.
This description comes directly from the study's public registry record.
Maria Zannes, JD · 505-400-9747 · mz@bioaffinitytech.com
Xavier Reveles, MS · 210-698-5334 · xr@bioaffinitytech.com
Always discuss trial participation with your own doctor first.
| Atlantic Respiratory Institute | Summit, New Jersey, United States | Recruiting |
| Radiology Associates of Albuquerque | Albuquerque, New Mexico, United States | Recruiting |
| South Texas Veterans Health Care System (STVHCS)/Audie L. Murphy Memorial Veterans Hospital | San Antonio, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT03457415