Seasonal Allergic Rhinitis
Conditions
Brief summary
Evaluation of the effect of fluticasone propionate vs placebo applied as nasal spray on the increase of allergen-specific serum IgE levels following nasal exposure to recombinant allergens. Nasal sprays will be applied for four weeks starting two weeks before nasal provocation and serum IgE levels will be followed during eight weeks after nasal provocation.
Interventions
DRUGFluticasone propionate
200 µg intranasal, 4 weeks, od.
DRUGPlacebo
Placebo intranasal spray
Sponsors
Allergy Centre Vienna West
Medical University of Vienna
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
* male or female 18-50 years of age * moderate to severe allergic rhinitis to grass and/or birch pollen for at least two seasons according to history * sensitization to rPhl p 5 and rBet v 1 as demonstrated by UniCAP within a range from 3.0-80 kUA/l and a positive (wheal diameter \>= 3 mm larger than the negative control and half of the histamine control) SPT with rPhl p 5 and rBet v 1 at 20 µg/ml * willingness to comply with the study protocol * written informed consent
Exclusion criteria
* perennial allergic rhinitis * history of asthma necessitating treatment * FEV1 \<70% of predicted value * abnormalities at auscultation of heart or lungs * history of anaphylaxis * severe atopic dermatitis * total serum IgE \>2000 kU/l * previous or ongoing immunotherapy (subcutaneous or sublingual) to grass or birch pollen * nasal provocation testing during the previous six month * known allergy/intolerance to fluticasone propionate or loratadine * known allergy/intolerance to cellulose, polysorbate, phenylethyl alcohol, benzalkonium chloride * contraindications for the use of INCS: * acute or chronic infections of the upper respiratory tract * surgery of the nose during the previous year * hypersensitivity to components of the drug * contraindications for nasal provocation test * acute rhinosinusitis * acute allergic reaction of the immediate type at other organs * nasal polyposis or significant nasal anatomical deformities * vasomotor rhinitis * autoimmune disease, chronic or acute infectious disease, malignancy * severe psychological disorder * treatment with systemic or topical (intranasal, inhaled, external) corticosteroids from 3 month prior to the study * treatment with other immunosuppressant drugs from 6 month prior to the study * treatment with antihistamines or disodium cromoglycate from 2 weeks prior to the study * treatment with intranasal adrenergic drugs from 3 days prior to the study * treatment with systemic adrenergic drugs * treatment with psychopharmacological drugs from 2 weeks prior to the study * cardiovascular or pulmonary disease * contraindication for adrenaline * participation in any other clinical trial within the previous 3 month * pregnant, lactating or sexually active women with childbearing potential who are not using a medically accepted birth control method * a mental condition rendering the subject unable to understand the nature, scope and possible consequences of the study, and/or evidence of an uncooperative attitude * known alcohol or drug addiction or abuse * unlikelihood to be able to complete the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Allergen specific IgE levels | 8 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Allergen specific IgG 1-4, IgM, IgA levels | 8 weeks |
Countries
Austria
Outcome results
None listed