Desensitizing treatments for dentin hypersensitivity: a randomized, split-mouth clinical trial
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
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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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 |
format |
article |
status_str |
publishedVersion |
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) |
instacron_str |
SBPQO |
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 |
_version_ |
1750318322877988864 |