Last updated: 11/07/2018 16:53:41
Title: A double-blind, randomized, placebo-controlled study of the efficacy and safety of once- versus twice-daily intranasal administration of aqueous fluticasone proprionate for two weeks in adult patients with seasonal allergic rhinitis
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Title: A double-blind, randomized, placebo-controlled study of the efficacy and safety of once- versus twice-daily intranasal administration of aqueous fluticasone proprionate for two weeks in adult patients with seasonal allergic rhinitis
Trial description: Title: A double-blind, randomized, placebo-controlled study of the efficacy and safety of once- versus twice-daily intranasal administration of aqueous fluticasone proprionate for two weeks in adult patients with seasonal allergic rhinitis
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Nathan R, Bronsky E, Fireman P, et al. A study of once versus twice-daily intranasal fluticasone propionate in the treatment of seasonal allergic rhinitis. J Allergy Clin Immunol 1990;85(1):163 (abstract)
Nathan RA, Bronsky EA, Fireman P, et al. Once daily fluticasone propionate aqueous nasal spray is an effective treatment for seasonal allergic rhinitis. Ann Allergy 1991;67:332-338
Medical condition
Rhinitis, Allergic, Seasonal
Product
fluticasone propionate
Collaborators
Not applicable
Study date(s)
N/A to December 1990
Type
Not applicable
Phase
2
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1990-01-12
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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