Actively Recruiting
Emphysema Research Registry; Screening Study and Genetic Testing
Led by University of Pittsburgh · Updated on 2025-09-25
3000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are gathering detailed information from people diagnosed with emphysema and related lung conditions like chronic obstructive pulmonary disease (COPD) and chronic bronchitis. This observational study aims to build a research registry to better understand emphysema and support the evaluation of new treatments. The registry also helps identify potential participants for future research. DNA samples will be collected to study genetic factors linked to COPD. Participants will undergo various tests and evaluations at the Emphysema/COPD Research Center. This includes answering respiratory questionnaires about symptoms and quality of life, performing lung function tests before and after inhaling a bronchodilator medicine called albuterol, providing blood samples for routine tests and genetic analysis, and measurements of leg muscle strength and body fat. Participants may also provide additional blood samples if they experience worsening COPD symptoms. During the study, participant information and test results will be securely stored and periodically updated. Assessments like pulmonary function, muscle strength, and body fat help researchers better understand emphysema's effects. The study allows ongoing communication with participants and maintains confidentiality by coding personal data. Participation includes informed consent, questionnaires, breathing tests, blood draws, and physical measurements, all conducted at the research center.
CONDITIONS
Brief Title
Emphysema Research Registry and Biosample Repository
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 21 years or older
- Diagnosis of COPD based on clinical history, lung function tests, or imaging
- History of at least 10 pack years of tobacco smoking
- Willingness to complete breathing questionnaires, lung function tests, blood draws, and physical measurements
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.
1 visit (in-person)
Duration - Indefinite
Participants provide personal and medical information, complete breathing questionnaires and lung function tests, have blood drawn, and undergo measurements of leg muscle strength and body fat. Participants are asked to contact the center during COPD exacerbations for additional blood samples.
Initial visit plus additional visits during COPD exacerbations as needed
Trial Site Locations
Total: 1 location
1
University of Pittsburgh Emphysema/COPD Research Center
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
Research Team
P
Paula Consolaro, CCRC
V
Vera Iouchmanov, BS
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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