Adolescent and Adult Subjects With Asthma and Seasonal Allergic Rhinitis Receiving Advair Diskus or Placebo
Withdrawn before enrolling · Not applicable · Has a placebo group
Conditions studied: Asthma, Seasonal Allergic Rhinitis
In brief
The four respiratory drugs being researched in this study have been approved by the US Food and Drug Administration (FDA) and are currently available by prescription at your drug store. One of the drugs is for the treatment of asthma alone, one is for treatment of SAR alone, and one is for treatment of both SAR and asthma. In addition, you will also receive one asthma rescue drug (albuterol) that is to be used for any breakthrough asthma symptoms that you may experience throughout the study. The purpose of this study is to see how well your asthma and SAR are controlled when taking one of the medicine combinations
Key facts
- Study ID
- NCT00385463
- Run by
- Creighton University
- People needed
- 0
- Starts
- 2006-04-01
- Expected to finish
- 2007-04-01
- Last updated by the study team
- 2016-06-16
Who can join
Age: 15 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Signed and dated written informed consent is obtained.
- Male or female
- 15 Years and older
- Diagnosis of persistent asthma for at least three months.
- 3 months prior and current use of specified asthma therapies
- FEV1 between 65-95% of predicted value
- Diagnosis of seasonal allergic rhinitis
- Active residence within geographical regions where exposure to relevant seasonal allergic is expected
You may not qualify if…
- Currently diagnosed with life-threatening asthma
- Asthma instability
- Concurrent respiratory disease
- Nasal obstruction
- Nasal history
- Certain concurrent conditions/diseases
- Drug allergy
- Respiratory tract infections
- Specific (listed in protocol) concurrent medications
- Systemic corticosteroids
Where it is running
- Creighton University — Omaha, Nebraska, United States
Full record on ClinicalTrials.gov
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