Abstract | PURPOSE: METHODS: This was a randomized, examiner-blind, parallel, two treatment group, stratified (by maximum baseline Schiff sensitivity score), 8-week clinical study carried out at a single site in 119 healthy subjects with at least two sensitive teeth, who met all study criteria at the screening and baseline visits. Clinical assessments of sensitivity to evaporative (air) [with Schiff sensitivity score and visual analogue scale (VAS)] and tactile (Yeaple probe) stimuli were employed to compare the efficacy of the test dentifrice containing 0.454% w/w stannous fluoride to the negative control dentifrice at reducing sensitivity after 4 and 8 weeks treatment. RESULTS: Of the 119 subjects randomized to study treatment, 113 completed the study. At 4 and 8 weeks, between treatment analyses found the test dentifrice to be significantly better than the negative control dentifrice in relieving dentin hypersensitivity for all measures (Schiff: P < 0.0001 at 4 and 8 weeks; VAS score: P = 0.0003 at 4 weeks, P < 0.0001 at 8 weeks; tactile threshold: P = 0.0138 at 4 weeks, P < 0.0001 at 8 weeks).
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Authors | Charles R Parkinson, Peter Jeffery, Jeffery L Milleman, Kimberly R Milleman, Stephen Mason |
Journal | American journal of dentistry
(Am J Dent)
Vol. 28
Issue 4
Pg. 190-6
(Aug 2015)
ISSN: 0894-8275 [Print] United States |
PMID | 26437498
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Dentifrices
- Tin Fluorides
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Topics |
- Adult
- Dentifrices
(therapeutic use)
- Dentin Sensitivity
- Female
- Humans
- Male
- Middle Aged
- Pain Management
(methods)
- Tin Fluorides
(therapeutic use)
- Young Adult
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