View Clinical Trial (Medical Research Study)
Study of the Effect of Fluticasone Furoate Nasal Spray on Spring Allergy Eye Symptoms - NCT00891436-60612(Clinical Trial 289940)
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Chicago |
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State:
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IL |
| Zip Code: |
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60612 |
| Conditions: |
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Allergic Conjunctivitis to Tree Pollen or Grass Pollen |
| Purpose: |
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Rationale and objectives:
Fluticasone furoate nasal spray (Veramyst) has been shown to improve ocular symptoms when
used for the treatment of seasonal allergic rhinitis during the ragweed pollen season.
Although this is the only published report of an intranasal corticosteroid shown to
effectively treat ocular symptoms, the mechanism has not been delineated. Furthermore, the
tears of patients with allergic conjunctivitis are known to have increased concentrations of
cytokines and allergic mediators.
The objective of this study is to determine if the positive effects of Veramyst nasal spray
on ocular symptoms is via the inhibition of allergic mediators in the eyes. The
investigators will conduct a double blind placebo controlled trial to determine if Veramyst
nasal spray decreases the amount of allergic mediators in the tears of subjects randomized
to Veramyst nasal spray versus placebo. The investigators will also compare the subjects'
symptoms to the amount of allergic mediators detected in their tears.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- a documented history of allergic rhinitis and conjunctivitis due to tree pollen and /
or grass pollen for two allergy seasons
- positive skin prick test to tree and / or grass
Exclusion Criteria:
- glaucoma
- cataracts
- acute or chronic sinusitis
- asthma
- chronic obstructive pulmonary disease
- physical nasal obstruction
- pregnant or breastfeeding
- have had a viral or bacterial infections within 2 weeks of the study commencement
- receiving allergen immunotherapy
- have used inhaled corticosteroids within 14 days prior to the study
- have used systemic corticosteroids within 30 days of the study
- travel outside of the geographic area during the 2 week study period
- use of contact lenses during the study period
- use of artificial tears during the study period
- use of eyewash irrigation during the study period
- use of lubricants during the study period |
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| Study is available at: |
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Rush University Medical Center Chicago, IL 60612 United States |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
this listing: |
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