Last updated: 11/07/2018 16:56:23
A double-blind, randomized, placebo-controlled study of the efficacy and safety of fluticasone propionate aqueous nasal spray versus placebo followed by a six-month open-label safety extension in subjects with perennial nonallergic 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, randomized, placebo-controlled study of the efficacy and safety of fluticasone propionate aqueous nasal spray versus placebo followed by a six-month open-label safety extension in subjects with perennial nonallergic rhinitis
Trial description: A double-blind, randomized, placebo-controlled study of the efficacy and safety of fluticasone propionate aqueous nasal spray versus placebo followed by a six-month open-label safety extension in subjects 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:
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Clinical publications:
Finn AF, Howland WC, Bronsky EA, Lumry WR, Pepsin PJ, Rogenes PR, Westlund R, Cook CK. Efficacy of three different dosing regimens of fluticasone propionate (FP) aqueous nasal spray in the treatment of perennial nonallergic rhinitis (PNAR). Allergy Clin Immunol 1997;99(No. 1, Part 2):S440 (abstract)
Pepsin PJ, Howland WC, Finn AF, Cox FM, Bowers BW, Montgomery E, Westlund R. Patient-rated overall treatment satisfaction and effectiveness with three dosing regimens of intranasal fluticasone propionate (FP) in perennial nonallergic rhinitis (PNAR). J Allergy Clin Immunol 1997;99(No. 1, Part 2):S442
Picone FJ, Pepsin PJ, Westlund R, Rogenes PR, Cook CK. Intranasal fluticasone propionate (FP) is effective in patients with perennial non-allergic rhinitis (NARES or Non-NARES). Ann of Allergy, Asthma, and Immunol 1998;80(1):111 (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
1996-01-05
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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