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Lung Macrophage Populations and Functions in Chronic Obstructive Pulmonary Disease (COPD)-Susceptible Smokers

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

Chronic Obstructive Pulmonary Disease (COPD) is a heterogeneous disease that affects only a fraction of those who smoke tobacco. The origin of this variability in susceptibility to develop COPD is unclear, but understanding its underlying biology has important implications for our ability to design suitable preventative and therapeutic strategies for its management. This Department of Defense (DOD) discovery research proposes to develop methodologies and generate preliminary data needed to lay the foundation for a large study that would investigate the underlying biological susceptibility of those who smoke tobacco to develop COPD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 75
Healthy Volunteers: t
View:

• Ages between 40 to 75 years old.

• History of at least 20 pack-years of smoking.

• No diagnosis of COPD or asthma.

• No spirometric evidence of airflow obstruction as determined by FEV1/FVC ratio ≥0.7.

• FEV1 and FVC \>lower limit of normal.

• Less than 1 pack-year history of tobacco smoking and no tobacco use within the past 12 months.

• Subjects will be divided into two groups by their RV/TLC:

⁃ Normal RV/TLC Group:

⁃ • Plethysmographic RV/TLC equal or less than lower limit of normal.

⁃ Abnormal RV/TLC Group:

⁃ • Plethysmographic RV/TLC higher than lower limit of normal.

Locations
United States
California
San Francisco VA Medical Center
RECRUITING
San Francisco
University of California, San Francisco
ACTIVE_NOT_RECRUITING
San Francisco
Zuckerberg San Francisco General Hospital and Trauma Center
ACTIVE_NOT_RECRUITING
San Francisco
Contact Information
Primary
Yorusaliem Abrham
yorusaliem.abrham@ucsf.edu
415-221-4810
Backup
Helen Lozier, B.A.
helen.lozier@ucsf.edu
(415) 609-6738
Time Frame
Start Date: 2021-03-01
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 40
Treatments
Normal RV/TLC Group:
Plethysmographic RV/TLC equal or less than lower limit of normal.
Abnormal RV/TLC Group:
Plethysmographic RV/TLC higher than lower limit of normal.
Sponsors
Leads: University of California, San Francisco
Collaborators: United States Department of Defense

This content was sourced from clinicaltrials.gov