A Two-week Study Assessing the Onset of Effect Questionnaire (OEQ) Administered Daily Versus Weekly 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) using a 1 week recall period versus a 1 day recall period.

Key facts

Study ID

NCT00449527

Run by

AstraZeneca

People needed

123

Starts

2007-03-01

Expected to finish

2007-08-01

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 — Tuscumbia, Alabama, United States
• Research Site — Fort Smith, Arkansas, United States
• Research Site — Long Beach, California, United States
• Research Site — Orange, California, United States
• Research Site — Riverside, California, United States
• Research Site — Sacramento, California, United States
• Research Site — San Diego, California, United States
• Research Site — San Jose, California, United States
• Research Site — Colorado Springs, Colorado, United States
• Research Site — Denver, Colorado, United States
• Research Site — Valrico, Florida, United States
• Research Site — River Forest, Illinois, United States
• Research Site — Council Bluffs, Iowa, United States
• Research Site — Topeka, Kansas, United States
• Research Site — Wichita, Kansas, United States
• Research Site — Bowling Green, Kentucky, United States
• Research Site — Florence, Kentucky, United States
• Research Site — Metairie, Louisiana, United States
• Research Site — City of Saint Peters, Missouri, United States
• Research Site — St Louis, Missouri, United States
• Research Site — Butte, Montana, United States
• Research Site — Omaha, Nebraska, United States
• Research Site — Papillion, Nebraska, United States
• Research Site — Las Vegas, Nevada, United States
• Research Site — Skillman, New Jersey, United States

Full record on ClinicalTrials.gov

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