Last updated: 11/07/2018 16:54:40
A double-blind, double-dummy, randomized, parallel group comparison of the efficacy and safety of fluticasone propionate aqueous nasal spray 200mcg QD versus astemizole 10mg QD versus placebo for four weeks in patients with seasonal allergic rhinitis.
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A double-blind, double-dummy, randomized, parallel group comparison of the efficacy and safety of fluticasone propionate aqueous nasal spray 200mcg QD versus astemizole 10mg QD versus placebo for four weeks in patients with seasonal allergic rhinitis.
Trial description: A double-blind, double-dummy, randomized, parallel group comparison of the efficacy and safety of fluticasone propionate aqueous nasal spray 200mcg QD versus astemizole 10mg QD versus placebo for four weeks in 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:
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Time perspective:
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Clinical publications:
Mackowiak J. Fluticasone propionate aqueous nasal spray (FP) improves rhinitis quality of life and reduces lost labor cost. Ann Allergy 1994;72:99 (abstract)
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
1992-10-07
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
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