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.author
Ojeda, Pedro
dc.contributor.author
Piqué i Clusella, Núria
dc.contributor.author
Alonso, Alicia
dc.contributor.author
Delgado, Julio (Delgado González)
dc.contributor.author
Feo, Francisco
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Igea, Juan Manuel
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Navarro, Ana
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Olaguibel, José María
dc.contributor.author
Subiza, Javier
dc.contributor.author
Nieto, Carles
dc.contributor.author
Andersson, Morgan
dc.date.issued
2015-01-28T15:39:29Z
dc.date.issued
2015-01-28T15:39:29Z
dc.date.issued
2013-08-27
dc.date.issued
2015-01-28T15:39:29Z
dc.identifier
1710-1492
dc.identifier
https://hdl.handle.net/2445/61967
dc.identifier
633816
dc.identifier
23981504
dc.description.abstract
Background: 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
8 p.
dc.format
application/pdf
dc.format
application/pdf
dc.language
eng
dc.publisher
BioMed Central
dc.relation
Reproducció del document publicat a: http://dx.doi.org/10.1186/1710-1492-9-32
dc.relation
Allergy, Asthma and Clinical Immunology, 2013, vol. 9, p. 32
dc.relation
http://dx.doi.org/10.1186/1710-1492-9-32
dc.rights
cc-by (c) Ojeda, Pedro et al., 2013
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biologia, Sanitat i Medi Ambient)
dc.subject
Assaigs clínics
dc.subject
Rinitis
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Al·lèrgia
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Emulsions (Farmàcia)
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Qualitat dels productes
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Clinical trials
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Rhinitis
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Allergy
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Emulsions (Pharmacy)
dc.subject
Quality of products
dc.title
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.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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