NCT Number: NCT00215449
Study in Patients With COPD
The purpose of this study is to determine the efficacy and safety of the investigational drug in the treatment of COPD in comparison with a placebo.
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Conditions
Age range
40 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Research Site, Bessemer, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Medical diagnosis of COPD
- Current or prior history of cigarette smoking
Exclusion criteria
- Medical diagnosis of asthma
- Chest x-ray (CXR) prior to Day 1 diagnostic of significant disease other than COPD
- Significant condition or disease other than COPD
Treatment and study plan
Primary outcomes
-
Measure of lung function
Secondary outcomes
-
Change in lung function, as well as vital signs
-
Physical Exam results, Adverse Event reporting, etc
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Lead sponsor
Dey
Industry
Registry information
Important dates
- Primary completion
- 2005
- Study completion
- 2006
- First posted
- Sep 22, 2005
- Registry last updated
- Nov 11, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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