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1 ice) and 2) placebo group (NSPT plus placebo dentifrice).
2 FMUD and daily use of a triclosan/copolymer dentifrice.
3 s microbiologic counts compared with placebo dentifrice.
4 ce to a positive control triclosan/copolymer dentifrice.
5 iodontal parameters than NSPT plus a placebo dentifrice.
6 the pyrophosphates to become soluble in the dentifrice.
7 may occur when pyrophosphates are added to a dentifrice.
8 f from DH of a zinc-carbonate hydroxyapatite dentifrice.
10 sing a double-mask, randomized design, three dentifrices: 1) containing 8% arginine and 1,450 ppm sod
11 n group (NSPT plus medicated 2% atorvastatin dentifrice) and 2) placebo group (NSPT plus placebo dent
12 etate-based dentifrice (group 2), and 29 the dentifrice based on zinc-carbonate hydroxyapatite (group
13 efore, was to determine efficacy of a SrAc2F dentifrice compared with KCl/MFP and a commercially avai
14 biologic effects of a commercially available dentifrice containing aloe vera on the reduction of plaq
15 Cl/MFP and a commercially available fluoride dentifrice containing sodium fluoride/sodium monofluorop
16 have demonstrated efficacy of desensitizing dentifrices containing strontium acetate/sodium fluoride
19 ice relative to a positive control triclosan dentifrice for prevention of clinical attachment loss (C
20 e only Food and Drug Administration-approved dentifrice for the treatment of plaque and gingivitis.
23 de and triclosan have been incorporated into dentifrice formulations and have been shown to be effect
24 individuals: 29 received the arginine-based dentifrice (group 1), 27 the strontium acetate-based den
25 ce (group 1), 27 the strontium acetate-based dentifrice (group 2), and 29 the dentifrice based on zin
28 s establish comparable benefits for the SnF2 dentifrice in preventing CAL and root caries versus the
29 % stannous fluoride/sodium hexametaphosphate dentifrice in reducing gingivitis compared to the triclo
31 nt study is to assess the effectiveness of a dentifrice medicated with 2% atorvastatin in improving c
32 ly assigned to a toothpaste regimen: control dentifrice (n = 21) or triclosan-containing dentifrice (
33 evaluates the effect of triclosan/copolymer dentifrice on the 6-month clinical response of patients
35 subjected to FMUD and daily use of a placebo dentifrice or to a test group (n = 15) subjected to FMUD
36 significant potential to be integrated into dentifrices or mouthrinses as an alternative non-fluorid
37 resent study, the use of triclosan/copolymer dentifrice promoted additional clinical benefits in the
38 e the efficacy of a stannous fluoride (SnF2) dentifrice relative to a positive control triclosan dent
40 This study documents that the three tested dentifrices significantly reduced DH after 3-day treatme
41 tifrice was tested versus a positive control dentifrice (sodium fluoride/0.30% triclosan/copolymer) i
42 hosphates have been approved as additives in dentifrices, these compounds along with the increased co
43 % stannous fluoride/sodium hexametaphosphate dentifrice to a positive control triclosan/copolymer den
44 he relative abilities of three desensitizing dentifrices to provide rapid relief of dentin hypersensi
47 e commercially available fluoride-containing dentifrice was as effective as the 2 desensitizing denti
49 % stannous fluoride/sodium hexametaphosphate dentifrice was tested against a commercially available p
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