Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial

Detalhes bibliográficos
Autor(a) principal: Camilotti,Veridiana
Data de Publicação: 2012
Outros Autores: Zilly,Juliana, Busato,Priscilla do Monte Ribeiro, Nassar,Carlos Augusto, Nassar,Patrícia Oehlmeyer
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Oral Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000300013
Resumo: The aim of this randomized, controlled, split-mouth, clinical study was to differentiate and clinically qualify the effectiveness of different desensitizing agents in the treatment of painful symptoms caused by cervical dentin hypersensitivity (CDH). Two hundred-and-fifty-two teeth of 42 patients were distributed into seven groups (n = 36): G1 - placebo; G2, G3, G4 and G6 - fluoride varnishes; G5 - sodium fluoride; G7 - potassium oxalate. Three applications were made one week apart. A three-score system (Alfa = 0, Bravo = 2, and Charlie = 3, respectively for no sensitivity, slight sensitivity and high sensitivity) was used to assess CDH after each application and after 30 days. The data were subjected to statistical analysis using the Kruskall-Wallis and Dun tests. After the second week, statistically significant differences were observed for all materials compared with the baseline. After 30 days, Group G7 had presented a significant gradual reduction along all the evaluated time intervals. It was concluded that all the desensitizing agents were capable of reducing dentin hypersensitivity, with the exception of the placebo and the sodium fluoride groups.
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spelling Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trialDentin SensitivityDentinFluoridesGingival RecessionThe aim of this randomized, controlled, split-mouth, clinical study was to differentiate and clinically qualify the effectiveness of different desensitizing agents in the treatment of painful symptoms caused by cervical dentin hypersensitivity (CDH). Two hundred-and-fifty-two teeth of 42 patients were distributed into seven groups (n = 36): G1 - placebo; G2, G3, G4 and G6 - fluoride varnishes; G5 - sodium fluoride; G7 - potassium oxalate. Three applications were made one week apart. A three-score system (Alfa = 0, Bravo = 2, and Charlie = 3, respectively for no sensitivity, slight sensitivity and high sensitivity) was used to assess CDH after each application and after 30 days. The data were subjected to statistical analysis using the Kruskall-Wallis and Dun tests. After the second week, statistically significant differences were observed for all materials compared with the baseline. After 30 days, Group G7 had presented a significant gradual reduction along all the evaluated time intervals. It was concluded that all the desensitizing agents were capable of reducing dentin hypersensitivity, with the exception of the placebo and the sodium fluoride groups.Sociedade Brasileira de Pesquisa Odontológica - SBPqO2012-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000300013Brazilian Oral Research v.26 n.3 2012reponame:Brazilian Oral Researchinstname:Sociedade Brasileira de Pesquisa Odontológica (SBPqO)instacron:SBPQO10.1590/S1806-83242012000300013info:eu-repo/semantics/openAccessCamilotti,VeridianaZilly,JulianaBusato,Priscilla do Monte RibeiroNassar,Carlos AugustoNassar,Patrícia Oehlmeyereng2012-05-23T00:00:00Zoai:scielo:S1806-83242012000300013Revistahttps://www.scielo.br/j/bor/https://old.scielo.br/oai/scielo-oai.phppob@edu.usp.br||bor@sbpqo.org.br1807-31071806-8324opendoar:2012-05-23T00:00Brazilian Oral Research - Sociedade Brasileira de Pesquisa Odontológica (SBPqO)false
dc.title.none.fl_str_mv Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
title Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
spellingShingle Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
Camilotti,Veridiana
Dentin Sensitivity
Dentin
Fluorides
Gingival Recession
title_short Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
title_full Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
title_fullStr Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
title_full_unstemmed Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
title_sort Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
author Camilotti,Veridiana
author_facet Camilotti,Veridiana
Zilly,Juliana
Busato,Priscilla do Monte Ribeiro
Nassar,Carlos Augusto
Nassar,Patrícia Oehlmeyer
author_role author
author2 Zilly,Juliana
Busato,Priscilla do Monte Ribeiro
Nassar,Carlos Augusto
Nassar,Patrícia Oehlmeyer
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Camilotti,Veridiana
Zilly,Juliana
Busato,Priscilla do Monte Ribeiro
Nassar,Carlos Augusto
Nassar,Patrícia Oehlmeyer
dc.subject.por.fl_str_mv Dentin Sensitivity
Dentin
Fluorides
Gingival Recession
topic Dentin Sensitivity
Dentin
Fluorides
Gingival Recession
description The aim of this randomized, controlled, split-mouth, clinical study was to differentiate and clinically qualify the effectiveness of different desensitizing agents in the treatment of painful symptoms caused by cervical dentin hypersensitivity (CDH). Two hundred-and-fifty-two teeth of 42 patients were distributed into seven groups (n = 36): G1 - placebo; G2, G3, G4 and G6 - fluoride varnishes; G5 - sodium fluoride; G7 - potassium oxalate. Three applications were made one week apart. A three-score system (Alfa = 0, Bravo = 2, and Charlie = 3, respectively for no sensitivity, slight sensitivity and high sensitivity) was used to assess CDH after each application and after 30 days. The data were subjected to statistical analysis using the Kruskall-Wallis and Dun tests. After the second week, statistically significant differences were observed for all materials compared with the baseline. After 30 days, Group G7 had presented a significant gradual reduction along all the evaluated time intervals. It was concluded that all the desensitizing agents were capable of reducing dentin hypersensitivity, with the exception of the placebo and the sodium fluoride groups.
publishDate 2012
dc.date.none.fl_str_mv 2012-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000300013
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242012000300013
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1806-83242012000300013
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Pesquisa Odontológica - SBPqO
publisher.none.fl_str_mv Sociedade Brasileira de Pesquisa Odontológica - SBPqO
dc.source.none.fl_str_mv Brazilian Oral Research v.26 n.3 2012
reponame:Brazilian Oral Research
instname:Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
instacron:SBPQO
instname_str Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
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institution SBPQO
reponame_str Brazilian Oral Research
collection Brazilian Oral Research
repository.name.fl_str_mv Brazilian Oral Research - Sociedade Brasileira de Pesquisa Odontológica (SBPqO)
repository.mail.fl_str_mv pob@edu.usp.br||bor@sbpqo.org.br
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