drugset / Trial / NCT01817790

Assessment of Fluticasone Propionate on Ocular Allergy Symptoms

NCT01817790 ↗

Phase 3 Completed 626 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blind

Summary

This study is designed to investigate the efficacy of fluticasone propionate (FP) on ocular symptoms associated with allergic rhinitis (AR).

Timeline

Start
2012-12
Primary completion
2013-02
Completion
2013-02

Outcome

Met primary endpoint

paper The least squares mean difference in the change from baseline of rTOSS was -0.36 (P = .002). PMID 25624132 ↗

paper Fluticasone was statistically significantly more efficacious in reducing the ocular symptoms of AR than placebo. PMID 25624132 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone propionate Other / unclassified 200 ug Intranasal