NCT Number: NCT00215384
Study in Patients With COPD
The purpose of this study is to determine which dose of the investigational drug is the most safe and effective compared to the control drug.
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Notify MeKey information
Conditions
Age range
50 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Research Site, Los Angeles, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-History of COPD and cigarette smoking
Exclusion criteria
- Clinical diagnosis of asthma.
- Chest X-ray that is diagnostic of a significant pulmonary disease other than COPD
- Disease of other major organ systems
Treatment and study plan
Primary outcomes
-
The primary outcome variable is the measure of lung function.
Secondary outcomes
-
Change in lung function will be examined as a secondary outcome, as well as vital signs, physical examination, adverse even reporting, etc.
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Lead sponsor
Dey
Industry
Registry information
Important dates
- Primary completion
- 2003
- Study completion
- 2005
- 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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