A Two-week Study Assessing the Onset of Effect Questionnaire Administered Pre-dose Versus Post-dose in Adult Subjects
Completed · Phase 3
Conditions studied: Asthma
In brief
The purpose of this study is to demonstrate whether subjects respond similarly to the Onset of Effect Questionnaire (OEQ) administered pre-dose versus post-dose, while receiving SYMBICORT® pMDI 80/4.5 μg x 2 actuations twice daily or budesonide HFA pMDI 80 μg x 2 actuations twice daily.
Key facts
- Study ID
- NCT00449501
- Run by
- AstraZeneca
- People needed
- 134
- Starts
- 2007-03-01
- Expected to finish
- 2007-11-01
- Last updated by the study team
- 2011-01-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or Female, > 18 years of age
- Mild to moderate asthma requiring treatment with an inhaled corticosteroid
- Diagnosis of asthma for at least 6 months
You may not qualify if…
- Subjects requiring treatment with systemic corticosteroids (e.g., oral, parenteral, ocular)
- Subjects with severe asthma, as judged by investigator
- Any significant disease or disorder that may jeopardize a subject's safety
Where it is running
- Research Site — Muscle Shoals, Alabama, United States
- Research Site — Little Rock, Arkansas, United States
- Research Site — Anaheim, California, United States
- Research Site — Los Angeles, California, United States
- Research Site — Palmdale, California, United States
- Research Site — Rolling Hills Estates, California, United States
- Research Site — Denver, Colorado, United States
- Research Site — Wheat Ridge, Colorado, United States
- Research Site — Stamford, Connecticut, United States
- Research Site — Wilmington, Delaware, United States
- Research Site — Miami, Florida, United States
- Research Site — Avon, Indiana, United States
- Research Site — Iowa City, Iowa, United States
- Research Site — Shawnee Mission, Kansas, United States
- Research Site — Mandeville, Louisiana, United States
- Research Site — Wheaton, Maryland, United States
- Research Site — Bay City, Michigan, United States
- Research Site — Chesterfield, Missouri, United States
- Research Site — Kansas City, Missouri, United States
- Research Site — McCook, Nebraska, United States
- Research Site — Scottsbluff, Nebraska, United States
- Research Site — Brick, New Jersey, United States
- Research Site — Princeton, New Jersey, United States
- Research Site — North Syracuse, New York, United States
- Research Site — Bismarck, North Dakota, United States
Full record on ClinicalTrials.gov
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