Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days

Abstract Objectives: To evaluate a 0.454% stannous fluoride/5% sodium tripolyphosphate (STP) toothpaste’s ability to provide relief from dentinal hypersensitivity (DH) applied using ‘focused brushing.’ Materials and methods: In two randomised, examiner-blind, parallel-group studies, a SnF2/STP tooth...

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Main Authors: Jonathan E. Creeth, Chhaju Goyal, Jimmy Qaqish, Robert Maclure, Jonathan S. Holt
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:BDJ Open
Online Access:https://doi.org/10.1038/s41405-021-00076-3
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spelling doaj-fcfb87ebf6bd4c2f9162289b5c3cd7a92021-07-18T11:11:20ZengNature Publishing GroupBDJ Open2056-807X2021-07-01711810.1038/s41405-021-00076-3Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 daysJonathan E. Creeth0Chhaju Goyal1Jimmy Qaqish2Robert Maclure3Jonathan S. Holt4GSK Consumer HealthcareAll Sum Research Centre LtdAll Sum Research Centre LtdIntertek Clinical Research ServicesIntertek Clinical Research ServicesAbstract Objectives: To evaluate a 0.454% stannous fluoride/5% sodium tripolyphosphate (STP) toothpaste’s ability to provide relief from dentinal hypersensitivity (DH) applied using ‘focused brushing.’ Materials and methods: In two randomised, examiner-blind, parallel-group studies, a SnF2/STP toothpaste was applied by brushing two selected sensitive teeth before 1 min whole-mouth brushing, compared to 1 min whole-mouth brushing only, with a negative control toothpaste. DH was assessed via evaporative (air) (Schiff scale) and tactile (Yeaple probe) stimuli after 7 and 14 d of twice-daily brushing. Results: In total, 141 (Study 1)/142 (Study 2) participants were randomised. In Study 1, the test treatment significantly reduced DH at 7/14 d versus baseline (7/14 d Schiff difference: −0.74 [−0.84,−0.65]/−1.39 [−1.54,−1.23]; tactile: 6.00 [4.88,7.13]/15.30 [13.34,17.26]); whereas the Control treatment did not (7/14 d Schiff difference −0.03 [−0.13,0.06]/−0.10 [−0.25,0.06]; tactile: 0.77 [−0.36,1.90]/0.77 [−1.20,2.74]). Differences between Test and Control were statistically significant (p < 0.0001 all cases). In Study 2, both treatments reduced DH compared to baseline by both measures, but there were no significant between-treatment differences. Toothpastes were generally well-tolerated. Discussion and conclusions: Previous studies and Study 1 support SnF2/5% STP toothpaste efficacy; Study 2 results may have been influenced by placebo/Hawthorne effects. DH study design needs to, where possible, negate such effects.https://doi.org/10.1038/s41405-021-00076-3
collection DOAJ
language English
format Article
sources DOAJ
author Jonathan E. Creeth
Chhaju Goyal
Jimmy Qaqish
Robert Maclure
Jonathan S. Holt
spellingShingle Jonathan E. Creeth
Chhaju Goyal
Jimmy Qaqish
Robert Maclure
Jonathan S. Holt
Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
BDJ Open
author_facet Jonathan E. Creeth
Chhaju Goyal
Jimmy Qaqish
Robert Maclure
Jonathan S. Holt
author_sort Jonathan E. Creeth
title Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
title_short Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
title_full Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
title_fullStr Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
title_full_unstemmed Efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
title_sort efficacy of an occluding toothpaste on dentinal hypersensitivity over 14 days
publisher Nature Publishing Group
series BDJ Open
issn 2056-807X
publishDate 2021-07-01
description Abstract Objectives: To evaluate a 0.454% stannous fluoride/5% sodium tripolyphosphate (STP) toothpaste’s ability to provide relief from dentinal hypersensitivity (DH) applied using ‘focused brushing.’ Materials and methods: In two randomised, examiner-blind, parallel-group studies, a SnF2/STP toothpaste was applied by brushing two selected sensitive teeth before 1 min whole-mouth brushing, compared to 1 min whole-mouth brushing only, with a negative control toothpaste. DH was assessed via evaporative (air) (Schiff scale) and tactile (Yeaple probe) stimuli after 7 and 14 d of twice-daily brushing. Results: In total, 141 (Study 1)/142 (Study 2) participants were randomised. In Study 1, the test treatment significantly reduced DH at 7/14 d versus baseline (7/14 d Schiff difference: −0.74 [−0.84,−0.65]/−1.39 [−1.54,−1.23]; tactile: 6.00 [4.88,7.13]/15.30 [13.34,17.26]); whereas the Control treatment did not (7/14 d Schiff difference −0.03 [−0.13,0.06]/−0.10 [−0.25,0.06]; tactile: 0.77 [−0.36,1.90]/0.77 [−1.20,2.74]). Differences between Test and Control were statistically significant (p < 0.0001 all cases). In Study 2, both treatments reduced DH compared to baseline by both measures, but there were no significant between-treatment differences. Toothpastes were generally well-tolerated. Discussion and conclusions: Previous studies and Study 1 support SnF2/5% STP toothpaste efficacy; Study 2 results may have been influenced by placebo/Hawthorne effects. DH study design needs to, where possible, negate such effects.
url https://doi.org/10.1038/s41405-021-00076-3
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