Vitamin D Plus Fluticasone Propionate
Completed · Phase 4 · Has a placebo group
Conditions studied: Seasonal Allergic Rhinitis
In brief
The objectives of this study would be to see if the addition of vitamin D to fluticasone propionate provides greater symptomatic relief in patients with seasonal allergic rhinitis compared to fluticasone propionate treatment alone.
Key facts
- Study ID
- NCT01103934
- Run by
- University of Chicago
- People needed
- 35
- Starts
- 2010-06-01
- Expected to finish
- 2011-07-01
- Last updated by the study team
- 2014-10-09
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males and females between 18 and 45 years of age.
- History of tree, grass and/or ragweed allergic rhinitis.
- Positive skin test to tree, grass and/or ragweed antigen.
- Positive response to screening nasal challenge.
You may not qualify if…
- Physical signs or symptoms suggestive of renal, hepatic or cardiovascular disease.
- Pregnant or lactating women.
- Upper respiratory infection within 14 days of study start.
Where it is running
- The University of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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