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[Charlotte] => https://www.survivornet.com/charlotte/
[Cleveland] => https://www.survivornet.com/cleveland/
[Columbus] => https://www.survivornet.com/columbus/
[Dallas / Ft. Worth] => https://www.survivornet.com/dallas-ftworth/
[Denver] => https://www.survivornet.com/denver/
[Detroit] => https://www.survivornet.com/detroit/
[Indianapolis] => https://www.survivornet.com/indianapolis-ovarian-cancer/
[Louisville] => https://www.survivornet.com/louisville/
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[Minneapolis] => https://www.survivornet.com/minneapolis/
[Nashville] => https://www.survivornet.com/nashville/
[Phoenix] => https://www.survivornet.com/phoenix/
[Portland] => https://www.survivornet.com/portland/
[Salt Lake City] => https://www.survivornet.com/salt-lake-city/
[San Antonio] => https://www.survivornet.com/san-antonio/
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A Registry for Patients With Multifocal Ground Glass Opacities (GGOs) Summary The purpose of this registry study is to actively monitor people with GGOs and collect information about them, so that investigators can learn more about these lesions and about the risk of developing lung cancer in study participants whose GGOs are being monitored in the active surveillance program.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Age greater than 18 years Have two or more GGOs on initial CT imaging GGOs must be measure ≤3.0 cm and ≥0.6 cm in the greatest dimension GGOs must be greater than half ground glass A biopsy is not necessary for inclusion in the trial. Biopsy of a GGO, even with a diagnosis of adenocarcinoma, does not necessarily preclude enrollment in this surveillance protocol. In other words, patients with a diagnosis of adenocarcinoma are still eligible, at the discretion of the clinician and/or investigator, if they meet the above criteria. Exclusion Criteria: Patients who are actively undergoing lung cancer treatment or have a history of lung cancer, except for cases of completely resected pathologic stage IA nonsmall cell lung cancer (NSCLC). Patients with stage IA NSCLC and multiple GGOs can enroll in this active surveillance protocol after complete resection of the NSCLC and confirmation of stage on final pathologic assessment. The presence of any solid lesion ≥0.6 cm suspicious for malignancy. Patients who are actively undergoing treatment for other malignancies
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There are 27 Locations for this study
Stanford University Medical Center (Data collection only) Stanford California, 94305, United States
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Hartford Healthcare Hartford Connecticut, 06102, United States
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Rush University Medical Center (Data collection only) Chicago Illinois, 60601, United States
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Massachusetts General Hospital Cancer Center Boston Massachusetts, 02114, United States
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Brigham and Women's Hospital Boston Massachusetts, 02115, United States
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University of Michigan Ann Arbor Michigan, 48109, United States
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Mayo Clinic Rochester Minnesota, 55905, United States
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George Washington University School of Medicine Saint Louis Missouri, 63110, United States
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Washington University School of Medicine Saint Louis Missouri, 63110, United States
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Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey, 07920, United States
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Memorial Sloan Kettering Monmouth Middletown New Jersey, 07748, United States
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Memorial Sloan Kettering Bergen Montvale New Jersey, 07645, United States
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Roswell Park Cancer Institute (Data Collection Only) Buffalo New York, 14263, United States
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Memorial Sloan Kettering Commack Commack New York, 11725, United States
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Memorial Sloan Kettering Westchester Harrison New York, 10604, United States
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Memorial Sloan Kettering Cancer Center New York New York, 10065, United States
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Memorial Sloan Kettering Nassau Uniondale New York, 11553, United States
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Duke University Medical Center Durham North Carolina, 27701, United States
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Lehigh Valley Health Network Allentown Pennsylvania, 18103, United States
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University of Pennsylvania (Data Collection Only) Philadelphia Pennsylvania, 19104, United States
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Thomas Jefferson University Hospital Philadelphia Pennsylvania, 19107, United States
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Fox Chase Cancer Center Philadelphia Pennsylvania, 19111, United States
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Allegheny-Singer Research Institute Pittsburgh Pennsylvania, 15212, United States
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University of Pittsburgh Medical Center Pittsburgh Pennsylvania, 15213, United States
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MD Anderson Cancer Center Houston Texas, 77030, United States
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Baylor University Medical Center Houston Texas, 77030, United States
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McMaster University (Data Collection Only) Hamilton Ontario, L8N 3, Canada
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University Health Network Toronto Ontario, M5G 2, Canada
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Centre Hospitalier de l'Université de Montreal Montréal Quebec, H2L 4, Canada
More Info How clear is this clinincal trial information?
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