Effect of 1.5% potassium oxalate on sensitivity control, color change, and quality of life after at-home tooth whitening: A randomized, placebo-controlled clinical trial

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MetadadosDescriçãoIdioma
Autor(es): dc.contributorUniversidade Federal do Pará (UFPA)-
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.creatorBarros, Antonia Patricia Oliveira-
Autor(es): dc.creatorda Silva Pompeu, Danielle-
Autor(es): dc.creatorTakeuchi, Elma Vieira-
Autor(es): dc.creatorde Melo Alencar, Cristiane-
Autor(es): dc.creatorAlves, Eliane Bemerguy-
Autor(es): dc.creatorSilva, Cecy Martins-
Data de aceite: dc.date.accessioned2025-08-21T20:51:38Z-
Data de disponibilização: dc.date.available2025-08-21T20:51:38Z-
Data de envio: dc.date.issued2023-07-29-
Data de envio: dc.date.issued2023-07-29-
Data de envio: dc.date.issued2022-10-31-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1371/journal.pone.0277346-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/246322-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/246322-
Descrição: dc.descriptionObjective This clinical trial evaluated the effect of 1.5% potassium oxalate (PO) in controlling sensitivity and color change after at-home tooth whitening. It also evaluated the influence of PO on health-related quality of life (HRQoL) and the degree of patient satisfaction after bleaching treatment. Materials and methods Fifty volunteers were randomized into two groups (n = 25): At-home bleaching gel with 22% carbamide peroxide for 45 min + placebo gel (GP) or 1.5% PO (GPO) for 10 min. The intensity of tooth sensitivity was assessed daily through the visual analog scale. The color analysis was performed three times: baseline, 21 days, and 1 month after the last application of the whitening gel. The impact of the oral condition on the patient’s quality of life (OIDP) was used to measure the impact caused by the whitening treatment in relation to the individuals’ ability to carry out their daily activities and its influence on HRQOL. Results No difference in tooth sensitivity was observed (p > 0.05). In addition, there was no difference in color change between groups (p > 0.05). However, there was an intragroup statistical difference throughout the evaluation period (p <0.05). The OIDP analysis showed a statistical difference between the groups (p > 0.05) and there was no difference between the groups regarding the degree of satisfaction with the bleaching (p > 0.05). Conclusions The 1.5% PO was effective in preventing sensitivity and did not interfere with tooth whitening. Desensitizing therapy had a positive impact on quality of life and patient satisfaction.-
Descrição: dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
Descrição: dc.descriptionUniversidade Federal do Pará-
Descrição: dc.descriptionSchool of Dentistry Federal University of Pará, Pará-
Descrição: dc.descriptionPostgraduate Program in Dentistry the Federal University of Pará, Pará-
Descrição: dc.descriptionAraraquara School of Dentistry Paulista State University (UNESP), Araraquara-
Descrição: dc.descriptionAraraquara School of Dentistry Paulista State University (UNESP), Araraquara-
Descrição: dc.descriptionCNPq: 157406/ 2020-2-
Idioma: dc.languageen-
Relação: dc.relationPLoS ONE-
???dc.source???: dc.sourceScopus-
Título: dc.titleEffect of 1.5% potassium oxalate on sensitivity control, color change, and quality of life after at-home tooth whitening: A randomized, placebo-controlled clinical trial-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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