NCT Number: NCT00215436
A Trial to Evaluate the Efficacy and Safety of Formoterol Fumarate in the Treatment of Patients With COPD
The purpose of this study is to determine the safety and efficacy of the investigational drug in comparison with a placebo.
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Notify MeKey information
Conditions
Age range
40 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Research Site, Jasper, 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 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
Sponsors and collaborators
Lead sponsor
Dey
Industry
Registry information
Official study title
A 12-week Double-Blind, Parallel-Group, Placebo- and Active- Controlled Trial to Evaluate the Efficacy and Safety of Formoterol Fumarate Inhalation Solution 20 Mcg in the Treatment of Patients With Chronic Obstructive Pulmonary Disease
Important dates
- Study start
- 2005
- Primary completion
- 2005
- Study completion
- 2006
- First posted
- Sep 22, 2005
- Registry last updated
- Nov 10, 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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