A randomized controlled clinical evaluation of desensitization efficacy of a newly developed toothpaste with highly stabilized SnF₂.

IF 0.9 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
American journal of dentistry Pub Date : 2023-08-01
Seongwoo Bak, Ji Young Kim, Brian Chung, Jonghoon Kim, Min-Jeong Cho, Wonho Ha, Kyu-Hwan Lee, Yongju Jung
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引用次数: 0

Abstract

Purpose: To assess the relief of dentin hypersensitivity of the new toothpaste with stabilized stannous fluoride (SnF₂) versus a marketed standard fluoride toothpaste as a negative control and a marketed anhydrous SnF₂ toothpaste as a positive control.

Methods: This was a single-centered, randomized, controlled, double blind, clinical trial. 96 participants with hypersensitivity were enrolled in this 4-week clinical study. Electrical stimulation and evaporative air tests were performed to evaluate the desensitization efficacy. Clinical assessments were made at baseline, and after 3 days, 1 week, 2 weeks and 4 weeks of twice-daily brushing. Additionally, the influence of Sn² ⁺ species on desensitization was evaluated using bovine dentin specimens treated with toothpaste.

Results: All 96 enrolled participants were randomized. 96 participants completed all evaluations. Participants had an average age (SD) of 47.0 (10.5) years; 45% of participants were female. Both SnF₂ toothpastes showed superior desensitization efficacy compared to the negative control toothpaste, the conventional sodium monofluorophosphate (SMFP) toothpaste, after a week. The new stabilized SnF₂ toothpaste demonstrated improved electrical stimulation benefits compared to the negative control toothpaste, with increases of 15.1% after 3 days, 34.2% after 1 week, 66.3% after 2 weeks, and 111.6% after 4 weeks. Additionally, it showed relative verbal evaluation scale (VES) benefits of 14.2% after 3 days, 37.6% after 1 week, 28.9% after 2 weeks, and 37.4% after 4 weeks. The stabilized SnF₂ toothpaste exhibited desensitization properties comparable to those of a commercial anhydrous SnF₂ toothpaste, which typically produces undesirable side effects in the mouth. Toothpastes containing 0.454 % SnF₂ exhibited perfect occlusion of dentin tubules.

Clinical significance: The stabilized 0.454% SnF₂ toothpaste exhibited significantly greater dentin hypersensitivity relief within only a week and comparable property to commercial anhydrous SnF₂ toothpaste.

新开发的高稳定SnF 2牙膏脱敏效果的随机对照临床评价。
目的:评估含有稳定氟化亚锡(SnF 2)的新型牙膏对牙本质过敏的缓解程度,与市场上销售的标准含氟牙膏作为阴性对照和市场上销售的无水SnF 2牙膏作为阳性对照进行比较。方法:单中心、随机、对照、双盲临床试验。96名过敏患者参加了为期4周的临床研究。通过电刺激和蒸发空气试验来评价脱敏效果。分别在基线、3天、1周、2周和4周后进行临床评估。另外,用牙膏处理过的牛牙本质样品,评价了Sn 2 +种类对脱敏效果的影响。结果:96名入组参与者均为随机化。96名参与者完成了所有评估。参与者的平均年龄(SD)为47.0(10.5)岁;45%的参与者是女性。两种SnF 2牙膏的脱敏效果在一周后均优于阴性对照牙膏(传统的单氟磷酸钠牙膏)。与阴性对照牙膏相比,新稳定的SnF 2牙膏的电刺激效果有所改善,3天后增加15.1%,1周后增加34.2%,2周后增加66.3%,4周后增加111.6%。3天、1周、2周、4周的相对言语评价量表(VES)改善率分别为14.2%、37.6%、28.9%和37.4%。稳定的SnF 2牙膏表现出与商业无水SnF 2牙膏相当的脱敏性能,后者通常在口腔中产生不良副作用。含0.454 % SnF₂的牙膏对牙本质小管具有良好的闭塞性。临床意义:稳定的0.454% SnF 2牙膏在一周内表现出明显更大的牙本质过敏缓解,其性能与市售无水SnF 2牙膏相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of dentistry
American journal of dentistry 医学-牙科与口腔外科
CiteScore
2.40
自引率
7.10%
发文量
57
审稿时长
1 months
期刊介绍: The American Journal of Dentistry, published by Mosher & Linder, Inc., provides peer-reviewed scientific articles with clinical significance for the general dental practitioner.
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