Diagnostic Study for Lung Cancer Detection Test
Early detection of lung cancer and early removal of the cancer nodules facilitates the diagnosis and treatment. However, not all nodules are malignant. Currently the standard method to diagnose lung cancer is to remove any suspicious nodules from the lung in a surgical procedure. This study is being conducted to evaluate the performance of a laboratory test to detect changes in lung cells that might be an early indicator of lung cancer. The test uses mucus (sputum) which is collected in a non-invasive method. This study will compare the results of the lung biopsy with the laboratory test to determine if the test can detect cancer or the lack of cancer. The laboratory test will not be shared with the treating physician or the patient as the current standard for lung cancer diagnosis is a biopsy. Approximately 330 patients will be enrolled in the study. There is one visit involved and includes the collection of a sputum specimen by coughing into a cup. The medical records of patients who are negative for cancer by biopsy will be reviewed for 2 years to detect any changes in diagnosis.
Checked against the public recordLast updated Jul 19, 2016 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Not specified
- Study type
- Observational
- Phase
- Not applicable
- Sponsor
- Bioview, Inc.
- Interventions being studied
- Not specified
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * Subjects with 0.8-3 cm solitary pulmonary nodules with high probability for malignancy * Candidate is scheduled to undergo lung biopsy procedure to determine clinical diagnosis, such as Bronchoscope biopsy, Electromagnetic Navigation Bronchoscopy, fiber optic Bronchoscopy, Needle biopsy, CT guided, Percutaneous Transthoracic Needle biopsy, Transthoracic Needle Biopsy, Open biopsy for Diagnostic Resection or Video-Assisted Thorascopic Surgery. * Candidate who is capable of undergoing sputum induction. * Ability to understand the investigational nature of the study and sign the informed consent. Exclusion Criteria: * Subjects who pose a high clinical risk for diagnostic bronchoscopy or transthoracic biopsy for definitive diagnosis. * Subjects already diagnosed with lung cancer, or previously treated for lung cancer. * Subjects who experienced pneumonia within last 12 weeks. * Subjects who experienced an acute respiratory infection within the last 2 weeks * Cases without sufficient documentation of diagnosis or follow-up will not be included. * Treatment for, or evidence of any cancer other than nonmelanoma skin cancer or carcinoma in situ within the last 3 years. * Subject who lack the capacity to consent.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- VA Greater Los Angeles Health SystemLos Angeles, California
- Frederick Memorial Hospital, Regional Cancer CenterFrederick, Maryland
- St. Luke's HospitalBethlehem, Pennsylvania
- Kaplan Medical CenterRehovot
- Tel-Aviv Sourasky Medical CenterTel Aviv
- Sheba Medical Center Thoracic Cancer Research and Detection CenterTel Litwinsky
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 19, 2016. Always confirm current availability with the study team.