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dc.contributor.authorZalacain-Vicuña, A.J.*
dc.contributor.authorNieto, C.*
dc.contributor.authorPicas, J.*
dc.contributor.authorMartínez, H.*
dc.contributor.authorBermejo, R.*
dc.contributor.authorCorrales, A.*
dc.contributor.authorCampos, F.F.*
dc.contributor.authorIgea, S.*
dc.contributor.authorOtero Espinar, Francisco*
dc.contributor.authorBriones, V.-P.*
dc.date.accessioned2025-09-09T10:25:24Z
dc.date.available2025-09-09T10:25:24Z
dc.date.issued2023
dc.identifier.citationZalacain-Vicuña AJ, Nieto C, Picas J, Martínez H, Bermejo R, Corrales A, et al. Efficacy and safety of a new medicated nail hydrolacquer in the treatment of adults with toenail onychomycosis: A randomised clinical trial. Mycoses. 2023;66(7):566-75.
dc.identifier.issn1439-0507
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/638bea72840d3a6d9ac831e6
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21418
dc.description.abstractBackground: A new water-soluble formulation with ciclopirox has shown a higher penetration than other ciclopirox nail lacquers currently marketed, thus providing a higher concentration of ciclopirox into the nail. Objective: To evaluate the efficacy and safety of a new ciclopirox nail hydrolacquer compared with its vehicle and an active comparator (hydroxypropyl chitosan-based 80 mg/g ciclopirox nail lacquer) for the treatment of toenail fungal infection. Methods: Phase III, multicenter, randomised, double-blind, clinical trial in patients with distal mild to moderate toenail onychomycosis due to dermatophyte fungi. Patients were randomised to apply topically a ciclopirox nail hydrolacquer, its vehicle or a reference product once daily for 48 weeks with a follow-up period of 4 weeks up to week 52. Results: A total of 381 patients were included. No statistically significant differences were observed between patient groups in the proportion of subjects achieving a complete cure. At week 52, a higher percentage of patients in the ciclopirox nail hydrolacquer group achieved a mycological cure (negative for culture and DTS/KOH test, with results: 32.0% ciclopirox nail hydrolacquer, 23.2% vehicle and 27% reference product, respectively), and similar results were found for improvement (mycological cure and reduction of diseased nail ?20%, with results: 27.2% ciclopirox nail hydrolacquer, 21.6% vehicle and 20.6% reference product, respectively). Regarding mycological results, only ciclopirox nail hydrolacquer demonstrated significant statistical superiority versus vehicle negativizing dermatophyte culture (p =.039) with no recurrences, relapses or re-infections in a four-week follow-up patients with complete cure. The safety profile was comparable to the vehicle and reference product and consistent with the previously reported. Conclusions: A new water-soluble formulation for a ciclopirox nail lacquer showed similar efficacy to the reference product to eradicate toenail onychomycosis and superiority in the mycological cure defined by negative culture, thus preventing reinfections and recurrences. Efficacy and safety data demonstrate the positive benefit-risk profile of this new topical antifungal preparation. [Correction added on 13 April 2023, after first online publication: The results and conclusions in the Abstract contained incorrect information and were revised in this version.].
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshHumans *
dc.subject.meshAdult *
dc.subject.meshOnychomycosis *
dc.subject.meshCiclopirox *
dc.subject.meshNails *
dc.subject.meshPyridones *
dc.subject.meshAdministration, Topical*
dc.subject.meshAntifungal Agents *
dc.subject.meshFoot Dermatoses *
dc.subject.meshWater *
dc.subject.meshTreatment Outcome *
dc.titleEfficacy and safety of a new medicated nail hydrolacquer in the treatment of adults with toenail onychomycosis: A randomised clinical trial
dc.typeArtigo
dc.authorsophosZalacain-Vicuña, A.J.; Nieto, C.; Picas, J.; Martínez, H.; Bermejo, R.; Corrales, A.; Campos, F.F.; Igea, S.; Otero-Espinar, F.J.; Briones, V.-P.
dc.identifier.doi10.1111/myc.13543
dc.identifier.sophos638bea72840d3a6d9ac831e6
dc.issue.number7
dc.journal.titleMycoses*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)
dc.page.initial566
dc.page.final575
dc.relation.publisherversionhttps://doi.org/10.1111/myc.13543
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Santiago
dc.subject.keywordIDIS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number66


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)