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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.
9 st a commercially available positive control dentifrice (0.30% triclosan/2.0% Gantrez copolymer).
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
17 efficacy between 1000- and 2500-ppm-fluoride dentifrices could be detected after 12 months.
18  dentifrice (n = 21) or triclosan-containing dentifrice ([CT] n = 18).
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.
21     A secondary objective was to compare the dentifrices for root caries remineralization.
22        First, tetrasodium pyrophosphate in a dentifrice forms a slightly alkaline solution upon oral
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
26                         In contrast, control dentifrice had little effect.
27 here is evidence that the use of arginine in dentifrices helps protect against caries.
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
30 rice was as effective as the 2 desensitizing dentifrices in alleviating CDS over time.
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
34 nticalculus component of most tartar control dentifrices on the market today.
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
39               The comparison among the three dentifrices showed that, after 3 days, there was an impr
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
45 n produced in this model with daily fluoride dentifrice treatments.
46 bjects were instructed to use their assigned dentifrice twice daily for 6 weeks.
47 e commercially available fluoride-containing dentifrice was as effective as the 2 desensitizing denti
48          NSPT plus 2% atorvastatin medicated dentifrice was more effective in improving clinical peri
49 % stannous fluoride/sodium hexametaphosphate dentifrice was tested against a commercially available p
50       A 0.454% SnF2/sodium hexametaphosphate dentifrice was tested versus a positive control dentifri
51 tients that were followed up to 8 weeks: all dentifrices were all highly efficacious.
52                                          All dentifrices were mostly effective to reduce DH: the perc

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