Last updated: 11/07/2018 16:54:16
A double-blind, randomized, placebo-controlled study of the efficacy and safety of two doses of fluticasone propionate aqueous nasal spray given twice daily versus placebo for four weeks in patients with perennial nonallergic rhinitis
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A double-blind, randomized, placebo-controlled study of the efficacy and safety of two doses of fluticasone propionate aqueous nasal spray given twice daily versus placebo for four weeks in patients with perennial nonallergic rhinitis
Trial description: A double-blind, randomized, placebo-controlled study of the efficacy and safety of two doses of fluticasone propionate aqueous nasal spray given twice daily versus placebo for four weeks in patients with perennial nonallergic 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:
Weakley S, Rogenes P, Field E. Intranasal fluticasone propionate treatment for perennial non-allergic rhinitis. J Allergy Clin Immunol 1991;87:218 (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
1990-01-09
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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