Biomarkers for Diagnosis of Lung Nodules

NCT ID: NCT01085864

Last Updated: 2025-03-20

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Total Enrollment: 550 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2010-03-17
• Study Completion Date: 2027-10-01

Brief Summary

A need exists for non-invasive testing to aid in clinical decision-making for Computerized Tomography (CT) scan detected lung nodules of indeterminate etiology. The investigators hypothesize that biomarkers detectable in blood, sputum or urine may be useful for guiding clinical decisions in the setting of CT detected lung nodules to determine which nodules are malignant and which are benign. The investigators also hypothesize that these biomarkers will decrease in concentration to the normal range after successful surgical treatment of malignant lung nodules.

Detailed Description

The Biomarkers for Diagnosis of Lung Nodules Study is a prospective study of a cohort of 500 individuals with lung nodules of indeterminate etiology that are identified by CT scans. Either biopsy or repeat CT scans must be clinically indicated to determine the etiology of the nodule. Patients will be asked to allow investigators access to CT scan images and spirometry data, and provide blood, sputum, urine, and exhaled breath samples over the course of the study. Patients will also be asked to allow investigators to access pathology records if a biopsy or surgical excision of the nodule is clinically indicated.

Conditions

Lung Abscess

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Study Groups

Patients with lung nodules on CT scan.

Patients with lung nodules on CT scan.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Adult 18-85 years of age

2. Patients referred to pulmonologists, oncologists, or thoracic surgeons for the evaluation of peripheral lung nodules found on CT scan.

3. Repeat CT scans, biopsy or surgical excision are clinically indicated to determine the etiology of the nodule.

4. One or more lung nodules must be between 8 mm and 30 mm in the greatest diameter.

5. Patients must be fully informed of the investigational nature of the procedure and sign an informed consent.

-

Exclusion Criteria

1. Lung nodules or masses greater than 30 mm in the greatest dimension.

2. Lung nodules that have solid calcification.

3. Lung nodules or masses with CT evidence of partial or complete obstruction of a lobar bronchus, main stem bronchus or the trachea.

4. No prior cancer with the exception of non-melanoma skin cancer.

5. Life expectancy of < 6 months

6. Any individual who does not give oral and written consent for participation -

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Colorado, Denver

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

York E Miller, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of Colorado, Denver

Locations

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

Countries

United States

Other Identifiers

09-1106.cc

Identifier Type: -

Identifier Source: org_study_id