An observational study in Pulmonary Disease, Chronic Obstructive, sponsored by GlaxoSmithKline. Completed at 44 sites in 12 countries. Open to participants aged 40 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-03-23.
Sponsored by GlaxoSmithKline · Observational
This is a 3 year longitudinal study to identify novel endpoints and compare these with standard measures such as forced expiratory volume in 1 second (FEV1) for their ability to measure and predict COPD (Chronic Obstructive Pulmonary Disease) severity and its progression over time. Control subjects (smokers and never smokers) will be recruited as comparators with the COPD subjects.
4,252 studies on the registry are indexed under Pulmonary Disease, Chronic Obstructive; 707 are open to participants now.
This study's enrollment of 2,747 is above the median of 183 across 1,099 observational studies indexed under Pulmonary Disease, Chronic Obstructive.
Browse Pulmonary Disease, Chronic Obstructive studies →GlaxoSmithKline is the lead sponsor of 3,647 studies on the registry; 118 are open to participants now.
Of its 264 completed or terminated interventional studies of FDA-regulated products, 239 (91%) have results posted.
Counted across the registry records on this site, refreshed daily.
COPD subjects and smoking and non-smoking controls
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Control Subjects - Current/Ex Smokers
Control Subjects - Non-smokers
Exclusion Criteria:
COPD Subjects
Control Subjects
Subjects with GOLD stage II-IV COPD
Other: Novel endpoint determination
Subjects with smoking history but normal lung function
Other: Novel endpoint determination
Normal healthy non-smokers
Other: Novel endpoint determination
Novel endpoint determination
Identifying new patient subtypes and endpoints for COPD
Time frame: 3 years
This study is completed, as verified in Mar 2017. You cannot join it, but the record below documents what was studied.
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Pulmonary Disease, Chronic Obstructive →