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NCT02504697Active, not recruiting

DECAMP-2: Screening of Patients With Early Stage Lung Cancer or at High Risk for Developing Lung Cancer

Detection of Early Lung Cancer Among Military Personnel Study 2 (DECAMP-2): Screening of Patients With Early Stage Lung Cancer or at High Risk for Developing Lung Cancer

Source: ClinicalTrials.gov · Last updated 1 Apr 2026

Brief summary (registry, in English)

The goal of this project is to improve lung cancer screening in high-risk individuals by identifying biomarkers of preclinical disease and disease risk that are measured in minimally invasive and non-invasive biospecimens. Existing biomarkers for lung cancer diagnosis as well as new biomarkers discovered specifically in this clinical setting will be examined. Biomarkers that identify individuals at highest risk for being diagnosed with lung cancer prior to the appearance of concerning symptoms could increase the utility of lung cancer surveillance and the efficiency of lung cancer chemoprevention clinical trials. Achieving these goals would improve the detection and treatment of early stage and incipient lung cancer, while restricting the risk of these procedures to those individuals who currently exhibit the early molecular warning signs of impending disease.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
665 (actual)
First submitted
27 May 2014
Start date
1 Sept 2011
Primary completion date
31 Dec 2027
Lead sponsor
Boston University
Diseases
Lung cancer
NCT number
NCT02504697

What you commit to

  • Study type: Observational
  • Participants enrolled: 665
  • From 1 Sept 2011 to the primary completion date, 31 Dec 2027
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Diagnosis of lung cancer prior to the current assessment (that is, patients are eligible if first lung cancer diagnosis has been recently confirmed by bronchoscopic biopsy and is leading to resection surgery, but not if this is not a first diagnosis);

Other illness

  • Contraindications to nasal brushing or fiberoptic bronchoscopy, including: ulcerative nasal disease, hemodynamic instability, severe obstructive airway disease (i.e., disease severity does not allow for bronchoscopic procedures), unstable cardiac or pulmonary disease, as well as other comorbidities leading to inability to protect airway, or altered level of consciousness;
  • Allergies to any local anesthetic that may be used to obtain biosamples in the study;

Other

  • Weight greater than that allowable by the CT scanner.

Who the study is looking for

  • Ages 50 to 79 years;
  • Smoking status: Current or former smoker (≥10 cigarettes/day for current smokers, or ≥20 pack years for former smoker who quit 20 years ago or less)
  • History of Chronic Obstructive Pulmonary Disease (COPD), emphysema, or at least one first-degree relative with a diagnosis of lung cancer;
  • Willing to undergo fiberoptic bronchoscopy;
  • Able to tolerate all biospecimen collection as required by protocol;
  • Able to comply with standard-of-care follow-up visits, including clinical exams, diagnostic work-ups, and imaging for a maximum of four years or until diagnosis of lung cancer;
  • Able to fill out Patient Lung History questionnaire;
  • Willing and able to provide a written informed consent.

Age in the registry: 50 years to 79 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Walter Reed National Military Medical Center
Coordinator of this site? Confirm its status
BethesdaUnited StatesUnknown status
Boston University Medical Center
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BostonUnited StatesUnknown status
Boston VA Research Institute, Inc
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BostonUnited StatesUnknown status
Health Research Inc. Roswell Park Division
Coordinator of this site? Confirm its status
BuffaloUnited StatesUnknown status
Dallas VA Research Corporation
Coordinator of this site? Confirm its status
DallasUnited StatesUnknown status
Denver Research Institute
Coordinator of this site? Confirm its status
DenverUnited StatesUnknown status
Regents of the University of California LA (Los Angeles VA Healthcare System)
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status
University of California Los Angeles Medical Center
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Los AngelesUnited StatesUnknown status
Middle Tennessee Research Institute (Vanderbilt University)
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status
University of Pennsylvania
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PhiladelphiaUnited StatesUnknown status
Trustees of University of Pennsylvania (Philadelphia VA Medical Center)
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Veterans Research Foundation of Pittsburgh
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PittsburghUnited StatesUnknown status
Naval Medical Center - Portsmouth
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PortsmouthUnited StatesUnknown status
San Antonio Military Medical Center
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San AntonioUnited StatesUnknown status
Naval Medical Center -San Diego
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San DiegoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.