The Effect of QVAR on Lung Functioning in Chronic Obstructive Pulmonary Disease
Stopped early · Not applicable
Conditions studied: COPD
In brief
This is an investigator-sponsored research study to evaluate if treatment with HFA-134a beclomethasone (QVAR) has an effect on peripheral (or outer) airway inflammation and airway "remodeling" or scarring in subjects with COPD. Approximately 20 subjects with COPD will participate for approximately 7 weeks, with 10 receiving an active (BDP) inhaler with HFA-134a and 10 receiving a placebo.
Key facts
- Study ID
- NCT00238082
- Run by
- National Jewish Health
- People needed
- 20
- Starts
- 1999-11-01
- Expected to finish
- 2005-02-01
- Last updated by the study team
- 2017-03-29
Who can join
Age: 45 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- COPD diagnosis
- FEV1/FVC<70%
- FEV1 50-80% predicted
- Albuterol response of <12% and <200mL or methacholine PC20 > 8mg/mL
- RV > 120% predicted
- DLCO < 80%
- smokers and nonsmokers
- Lower age limit 45 years
You may not qualify if…
- Asthma
- Other chronic airway or parenchymal lung disease
- Other comorbid illness (including but not limited to DM, MI or CAD-related intervention in 6 months, neurologic disease, syncope)
- Use of any steroid (oral, IV, nasal, pulmonary) within 12 weeks
- Use of theophylline, leukotriene modifiers within 12 weeks
- Use of long-acting beta-agonists (formoterol, salmeterol) or anticholinergic (tiotropium)
Where it is running
- National Jewish Medical and Research Center — Denver, Colorado, United States
Full record on ClinicalTrials.gov
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