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Dentifrice Abrasivity and Cervical Dentinal Hypersensitivity. Results 12 Weeks Following Cessation of 8 Weeks' Supervised Use
Author(s) -
Gillam D.G.,
Newman H.N.,
Bulman J.S.,
Davies E.H.
Publication year - 1992
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.1992.63.1.7
Subject(s) - dentifrice , medicine , dentistry , visual analogue scale , strontium chloride , tooth sensitivity , anesthesia , chemistry , strontium , inorganic chemistry , fluoride , organic chemistry
F ollowing an 8‐week controlled investigation of 2 strontium chloride hexahydrate dentifrices (SCH) of differing abrasivity, 2 groups of 20 subjects each, with cervical dentinal hypersensitivity, were re‐examined at 20 weeks; that is, 12 weeks after the active period. The examination procedures were conducted in the same manner as in the main clinical trial. Sensitivity levels were assessed by 2 instrument methods: tactile (Yeaple probe), and cold air (dental air syringe), and by subjective perception of pain by means of a Visual Analogue Scale. The results from these methods of assessment demonstrated that 12 weeks following the cessation of 8 weeks' controlled use of standard and low abrasive SCH dentifrices, sensitivity levels reversed only slightly in both groups and, overall, sensitivity remained significantly lower than at baseline. The abrasivity of the dentifrice did not affect the desensitivity activity. J Periodontol 1992; 63:7–12 .

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