首页> 外文期刊>American journal of dentistry >A randomized, controlled comparison of two professional dentin desensitizing agents immediately post-treatment and 2 months post-treatment
【24h】

A randomized, controlled comparison of two professional dentin desensitizing agents immediately post-treatment and 2 months post-treatment

机译:两种专业牙本质脱敏剂的随机受控比较后治疗后治疗后2个月

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: To compare the desensitizing effects of two different marketed professional dentin hypersensitivity treatments, a 5% sodium fluoride varnish and an oxalic acid/potassium salt solution, in a single-center, randomized, controlled, subject-blind pilot study. Methods: A total of 22 subjects with dentin hypersensitivity on at least two teeth were recruited from a general dentistry practice and randomized 1:1 to treatment with a 5% sodium fluoride varnish (Acclean Fluoride Varnish) group or a 3% oxalic acid/potassium salt solution (Super Seal Desensitizer). The study population was predominantly female (91%) and Caucasian (77%). The mean age was 46.4 years, with ages ranging from 18-73 years. Dentin hypersensitivity was assessed after an air blast challenge by the examiner (Schiff Index Sensitivity Scale) and by the subject [Visual Analog Scale (VAS)] for each tooth tested. Hypersensitivity was assessed immediately post-treatment and at 2 months post-treatment. Results: For the sodium fluoride varnish group, the mean Schiff score decreased 61% from baseline immediately post-treatment (P= 0.0006) and 41% at Month 2 (P= 0.0069). For the oxalic acid/potassium salt solution group, the mean Schiff score decreased 33% from baseline immediately post-treatment (P= 0.0305) and 29% at Month 2. Similarly, the mean VAS scores in the sodium fluoride varnish group decreased 41% from baseline immediately post-treatment (P= 0.0030) and 34% at Month 2 (P= 0.0275). The mean VAS scores in the oxalic acid/potassium salt solution group decreased 35% from baseline immediately post-treatment (P= 0.0168) and 33% at Month 2 (P= 0.0283). An analysis of covariance found no statistically significant between-group differences in mean Schiff scores or VAS scores immediately post-treatment or at Month 2. Both treatments were well tolerated. There were no reported adverse events in either treatment group.
机译:目的:比较两种不同营销专业牙本质过敏治疗,5%氟化钠清漆和草酸/钾盐溶液的脱敏效应,在单一中心,随机,控制,受理盲试点研究中。方法:从一般牙科实践中招募了至少两颗牙齿上的22例牙本质过敏的受试者,并随机1:1用5%氟化钠清漆(轴进氟氟化芳烃)基团或3%草酸/钾来治疗盐溶液(超密封剂)。研究人群主要是女性(91%)和高加索人(77%)。平均年龄为46.4岁,年龄在18-73岁之间。在检查者(Schiff指数敏感度尺度)和受试者[视觉模拟量表]对测试后的每颗牙齿的气出攻击后评估牙本质超敏反应。在治疗后立即评估过敏,在治疗后2个月评估。结果:对于氟化钠清漆组,平均席克夫得分从基线下降61%,立即治疗后(P = 0.0006)和41%(P = 0.0069)。对于草酸/钾盐溶液组,平均Schiff得分从基线下降33%,立即治疗后(P = 0.0305)和29%。类似,氟化钠清漆组的平均VAS分数降低了41%从基线立即治疗后(P = 0.0030)和34%在第2月(P = 0.0275)。草酸/钾盐溶液组中的平均VAS评分在治疗后立即从基线下降了35%(P = 0.0168)和33%(P = 0.0283)。对协方差的分析发现,在治疗后或在第2个月内立即进行平均席夫评分或VAS分数的组间差异没有统计学意义。两种治疗均可耐受良好。任何治疗组都没有报告的不良事件。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号