Last updated: 11/07/2018 17:07:18
The effect of intranasal fluticasone propionate on the recovery of proinflammatory cytokines in the nasal secretions following allergen challenge
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: The effect of intranasal fluticasone propionate on the recovery of proinflammatory cytokines in the nasal secretions following allergen challenge
Trial description: The effect of intranasal fluticasone propionate on the recovery of proinflammatory cytokines in the nasal secretions following allergen challenge
Primary purpose:
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Trial design:
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Masking:
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Allocation:
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Primary outcomes:
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Secondary outcomes:
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Interventions:
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Enrollment:
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Primary completion date:
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Observational study model:
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Time perspective:
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Clinical publications:
Weido AJ, Reece LM, Alam R, Cook CK, Sim TC. Intranasal fluticasone propionate inhibits recovery of chemokines and other cytokines in nasal secretions in allergen-induced rhinitis. Ann of Allergy, Asthma, and Immunol 1996;77:407-415;
Weido AJ, Reece LM, Alam R, et al. Intranasal fluticasone propionate (FP) inhibits recovery of IL-1B, IL-6, GM-CSF, and Chemokines in nasal secretions (NS) in allergy-induced rhinitis. J Allergy Clin Immunol 1995;95:389 (abstract);
Weido, AJ, Reece LM, Alam R, et al. Secretion profile of chemokines in early and late phase responses in the nasal mucosa: influence of topical steroid therapy. Ann Allergy 1996;76:81 (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
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Recruitment status
Study complete
Actual primary completion date
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Actual study completion date
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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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