Specimen Banking From Patients With Lung Cancer
2 other identifiers
observational
2,000
1 country
1
Brief Summary
The primary objective of the protocol is to develop a comprehensive specimen banking program from patients with lung cancer for future translation research, which will enable the investigators to detect lung cancer earlier, develop better therapies and explore screening and prevention strategies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2005
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 3, 2005
CompletedFirst Submitted
Initial submission to the registry
April 17, 2012
CompletedFirst Posted
Study publicly available on registry
April 26, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2035
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2035
January 29, 2026
January 1, 2026
29.7 years
April 17, 2012
January 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Development of a comprehensive specimen banking program from patients with lung cancer for future translational research.
No statistical analysis will be applied to the overall collection of samples. Rather, each project that utilized tissue bank resources will require an appropriate statistical plan to be submitted along with the initial tissue request.
6 years
Study Arms (1)
Diagnosis/treatment of lung cancer
Specimen Banking
Eligibility Criteria
Subjects who are undergoing further testing for the diagnosis or treatment of lung cancer.
You may qualify if:
- Subjects who are undergoing further testing for the diagnosis or treatment of lung cancer.
- Oral and written informed consent
You may not qualify if:
- \. Any individual who does not give oral and written consent for participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Colorado, Denverlead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
University of Colorado Cancer Center
Aurora, Colorado, 80045, United States
Biospecimen
Tissue, blood, urine, and sputum, breath
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Adriaan VanBokhoven, PhD
University of Colorado, Denver
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 17, 2012
First Posted
April 26, 2012
Study Start
November 3, 2005
Primary Completion (Estimated)
July 1, 2035
Study Completion (Estimated)
July 1, 2035
Last Updated
January 29, 2026
Record last verified: 2026-01