A topical microemulsion for the prevention of allergic rhinitis symptoms: results of a randomized, controlled, double-blind, parallel group, multicentre, multinational clinical trial (Nares study)

dc.contributor.authorOjeda, Pedro
dc.contributor.authorPiqué i Clusella, Núria
dc.contributor.authorAlonso, Alicia
dc.contributor.authorDelgado, Julio (Delgado González)
dc.contributor.authorFeo, Francisco
dc.contributor.authorIgea, Juan Manuel
dc.contributor.authorNavarro, Ana
dc.contributor.authorOlaguibel, José María
dc.contributor.authorSubiza, Javier
dc.contributor.authorNieto, Carles
dc.contributor.authorAndersson, Morgan
dc.date.accessioned2015-01-28T15:39:29Z
dc.date.available2015-01-28T15:39:29Z
dc.date.issued2013-08-27
dc.date.updated2015-01-28T15:39:29Z
dc.description.abstractBackground: Since barrier protection measures to avoid contact with allergens are being increasingly developed, we assessed the clinical efficacy and tolerability of a topical nasal microemulsion made of glycerol esters in patients with allergic rhinitis. Methods: Randomized, controlled, double-blind, parallel group, multicentre, multinational clinical trial in which adult patients with allergic rhinitis or rhinoconjunctivitis due to sensitization to birch, grass or olive tree pollens received treatment with topical microemulsion or placebo during the pollen seasons. Efficacy variables included scores in the mini-RQLQ questionnaire, number and severity of nasal, ocular and lung signs and symptoms, need for symptomatic medications and patients" satisfaction with treatment. Adverse events were also recorded. Results: Demographic characteristics were homogeneous between groups and mini-RQLQ scores did not differ significantly at baseline (visit 1). From symptoms recorded in the diary cards, the ME group showed statistically significant better scores for nasal congestion (0.72 vs. 1.01; p = 0.017) and mean total nasal symptoms (0.7 vs. 0.9; p = 0.045). At visit 2 (pollen season), lower values were observed in the mini-RQLQ in the ME group, although there were no statistically significant differences between groups in both full analysis set (FAS) and patients completing treatment (PPS) populations. The results obtained in the nasal symptoms domain of the mini-RQLQ at visit 2 showed the highest difference (−0.43; 95% CI: -0.88 to 0.02) for the ME group in the FAS population. The topical microemulsion was safe and well tolerated and no major discomforts were observed. Satisfaction rating with the treatment was similar between the groups. Conclusions: The topical application of the microemulsion is a feasible and safe therapy in the prevention of allergic symptoms, particularly nasal congestion.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec633816
dc.identifier.issn1710-1492
dc.identifier.pmid23981504
dc.identifier.urihttps://hdl.handle.net/2445/61967
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1186/1710-1492-9-32
dc.relation.ispartofAllergy, Asthma and Clinical Immunology, 2013, vol. 9, p. 32
dc.relation.urihttp://dx.doi.org/10.1186/1710-1492-9-32
dc.rightscc-by (c) Ojeda, Pedro et al., 2013
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Biologia, Sanitat i Medi Ambient)
dc.subject.classificationAssaigs clínics
dc.subject.classificationRinitis
dc.subject.classificationAl·lèrgia
dc.subject.classificationEmulsions (Farmàcia)
dc.subject.classificationQualitat dels productes
dc.subject.otherClinical trials
dc.subject.otherRhinitis
dc.subject.otherAllergy
dc.subject.otherEmulsions (Pharmacy)
dc.subject.otherQuality of products
dc.titleA topical microemulsion for the prevention of allergic rhinitis symptoms: results of a randomized, controlled, double-blind, parallel group, multicentre, multinational clinical trial (Nares study)
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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