Actively Recruiting
Thoracic Specimen Registry at Mayo Clinic to Support Research on Lung and Other Thoracic Diseases
Led by Mayo Clinic · Updated on 2026-01-16
7000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are establishing a Thoracic Specimen Registry to support research on lung cancer and other diseases affecting the chest area, such as mediastinal and pleural tumors, lung transplants, and other thoracic cancers. The registry aims to improve understanding of causes, early detection, clinical care, and outcomes for these conditions by collecting a wide range of specimens from patients with thoracic diseases or at high risk for such conditions. The registry collects various types of specimens including blood, bronchoalveolar lavage fluid, pleural fluid, surgical tissues, biopsies, and touch prep samples. These specimens are stored centrally at Mayo Clinic and managed by a dedicated steering committee. This resource will facilitate future research studies and clinical trials focused on discovering new markers for screening and diagnosis, as well as developing improved treatments and preventive strategies. Participants provide specimens during their routine clinical care related to thoracic diseases, and their samples are stored for research purposes. The primary outcome is the ongoing development of a comprehensive thoracic specimen repository over approximately 10 years. This registry supports long-term research and does not involve experimental treatments. Participants remain under their usual care throughout the study period.
CONDITIONS
Brief Title
Thoracic Specimen Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subject must be over 18 years of age
- Presumed or known thoracic diseases including but not limited to thoracic neoplasms, interstitial lung diseases, chronic obstructive pulmonary disease, thoracic infections, thoracic malignancies, or other cancers metastatic to the thoracic cavity
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 10 years
Participants provide blood, tissue, and fluid specimens to support research on thoracic diseases.
Specimen collection visits as needed during the study period
Trial Site Locations
Total: 1 location
1
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
A
Aaron Bungum
K
Karlyn Pierson, RN
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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