Toothpastes containing potassium nitrate alone versus potassium nitrate combined with aluminum lactate in reducing dentin hypersensitivity: a randomized controlled trial.

IF 3.1 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Kohei Ishii, Taiki Suzuki, Chika Akabane, Gotaro Iizumi, Naho Suzuki, Yasushi Fukuda, Kenta Suzuki, Naoko Kawaguchi, Ruixue Zhu, Debao Li, Zhi Zhou, Deyu Hu
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引用次数: 0

Abstract

Objective: Dentin hypersensitivity (DH) is a common clinical condition characterized by transient, sharp pain arising from exposed dentinal tubules in response to external stimuli. The aim of this study was to evaluate and compare the efficacy of two toothpaste formulations: one containing 5% potassium nitrate alone and another combining 5% potassium nitrate with 2.18% aluminum lactate.

Materials and methods: This was a parallel-group, randomized, double-blind, negative-control trial with 127 participants. Participants were randomly assigned to three groups (two test and one placebo). The Dentin Sensitivity Index (DSI) was assessed under tactile and air stimulation at baseline, immediately after brushing, and at 2 weeks, 4 weeks, 4 weeks plus 24 h, and 8 weeks.

Results: Compared with baseline, both test groups showed statistically significant reductions in DSI for both tactile and air stimulation at all time points immediately after use. From 2 weeks onward, the DSI of both test groups was significantly lower than that of the placebo group at all evaluated time points. Furthermore, the toothpaste containing 5% potassium nitrate combined with 2.18% aluminum lactate exhibited a greater effect than the potassium nitrate alone at specific time points: 4 weeks for air stimulation, 4 weeks plus 24 h for tactile stimulation, and 8 weeks for both types of stimulation.

Conclusions: Both toothpaste formulations-5% potassium nitrate alone and 5% potassium nitrate combined with 2.18% aluminum lactate-demonstrated significant efficacy in reducing dentin hypersensitivity, with the combination showing greater improvement at several time points.

Clinical trial registration: Trial registration: ISRCTN80733222.

单独含有硝酸钾的牙膏与硝酸钾联合乳酸铝减少牙本质过敏:一项随机对照试验。
目的:牙本质过敏(DH)是一种常见的临床症状,其特征是由于暴露的牙本质小管对外界刺激的反应而引起短暂的尖锐疼痛。本研究的目的是评价和比较两种牙膏配方的疗效:一种是单独含有5%硝酸钾,另一种是将5%硝酸钾与2.18%乳酸铝混合。材料和方法:这是一项平行组、随机、双盲、负对照试验,共有127名参与者。参与者被随机分为三组(两组测试和一组安慰剂)。在基线、刷牙后立即、2周、4周、4周加24小时和8周的触觉和空气刺激下评估牙本质敏感指数(DSI)。结果:与基线相比,两个试验组在使用后立即进行触觉和空气刺激的所有时间点的DSI均有统计学意义上的显著降低。从2周开始,两个试验组在所有评估时间点的DSI均显著低于安慰剂组。此外,在特定的时间点上,含有5%硝酸钾和2.18%乳酸铝的牙膏在空气刺激4周、触觉刺激4周加24小时、两种刺激8周的效果都比单独使用硝酸钾的效果更好。结论:5%硝酸钾单用和5%硝酸钾联合2.18%乳酸铝两种牙膏配方均能显著降低牙本质过敏反应,且在多个时间点上均有较大改善。临床试验注册:试验注册号:ISRCTN80733222。
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
BDJ Open
BDJ Open Dentistry-Dentistry (all)
CiteScore
3.70
自引率
3.30%
发文量
34
审稿时长
30 weeks
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