首页> 外文期刊>American journal of dentistry >Efficacy of stabilized chlorine dioxide-based unflavored mouthwash in reducing oral malodor: An 8-week randomized controlled study
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Efficacy of stabilized chlorine dioxide-based unflavored mouthwash in reducing oral malodor: An 8-week randomized controlled study

机译:稳定的二氧化氯无灌注漱口水在减少口服恶臭的疗效:8周随机对照研究

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摘要

Purpose: To evaluate the efficacy of a mouthwash containing stabilized chlorine dioxide in reducing oral malodor when used as an adjunct to tooth brushing compared with the use of a placebo mouthwash. Methods: This 8 week study in healthy subjects with clinically diagnosed intrinsic oral malodor was a 2-way crossover, double-blind, randomized, and controlled trial design, which was conducted at a single site. Subjects were randomized to receive either unflavored, non-fluoridated, and alcohol-free mouthwash containing 0.1% stabilized chlorine dioxide or a placebo mouthwash with identical bottle packaging. Both groups were provided with the same toothpaste and toothbrush. Subjects consented to the 8-week participation and were instructed to use their allocated treatment twice daily. In Phase I, quantified odor intensity [measured by an organoleptic intensity rating scale of 0-5, with 0=malodor cannot be detected and 5=very strong malodor] was independently evaluated by three calibrated judges at baseline, and after 1, 2, and 3 weeks of treatment. Following a 2-week washout period, Phase II initiated with the redistribution of test products. The subjects' organoleptic scores were assessed by the calibrated judges at baseline, and 6, 7, and 8 weeks of treatment. Results: A total of 50 subjects were enrolled and randomized into the two groups. Of these, 47 subjects completed the study. The baseline organoleptic intensity scores for both groups during Phase I and Phase II were not significantly different (P= 0.224, P = 0.071, respectively). At all visits, the organoleptic scores for the placebo rinse group during both Phase I and Phase II were not significantly different. During Phase I, the mean of individual organoleptic change scores from the stabilized chlorine dioxide rinse group were significantly different from the baseline at the last two follow-up visits: Week 1 (P = 0.088), Week 2 (P = 0.001), Week 3 (P = 0.1 x10(-3)). During Phase II, the mean of individual organoleptic change scores from the stabilized chlorine dioxide rinse group were also significantly different from the baseline at the last two follow-up visits: Week 6 (P = 0.120), Week 7 (P = 0.004), Week 8 (P = 0.002).
机译:目的:评估含有稳定氯二氧化氯的疗效在用作牙齿刷涂时减少口服恶臭时的疗效。方法:在临床诊断的内在口腔恶臭的健康受试者中,这8周的研究是一种双向交叉,双盲,随机和受控试验设计,该设计在单一地点进行。受试者随机接受含有0.1%稳定的二氧化氯或具有相同瓶包装的安慰剂漱口水的无含油,不氟化的和无氟化物的漱口水。两组都配有相同的牙膏和牙刷。受试者同意为期8周的参与,并指示每天两次分配治疗。在I阶段I中,量化气味强度[通过0-5的感官强度额定量表测量,不能检测到0 =恶臭,并且5 =非常强的恶臭]独立地通过基线的三个校准的判断进行了单独评估,而1,2之后,和3周的治疗。在2周的洗涤期后,II期通过试验产品的重新分配启动。受试者的感官分数由基线的校准法官进行评估,6,7和8周治疗。结果:共注册了50个受试者并随机分为两组。其中,47名受试者完成了这项研究。在I相和II期间两组的基线感官强度分数没有显着差异(P = 0.224,分别为0.071)。在所有访问中,在I相和II期间安慰剂漂洗组的感官分数没有显着差异。在第I阶段期间,稳定氯二氧化氯漂洗组的个体感官变化分数的平均值与最后两个后续访问的基线显着不同:第1周(P = 0.088),第2周(P = 0.001)周3(p = 0.1 x10(-3))。在II期期间,稳定氯二氧化氯漂洗组的个体感官变化分数的平均值也与最后两个后续访问的基线有显着不同:第6周(P = 0.120),第7周(P = 0.004),第8周(P = 0.002)。

著录项

  • 来源
    《American journal of dentistry》 |2018年第6期|共4页
  • 作者单位

    Loma Linda Univ Sch Dent Dent Res Ctr Chan Shun Pavil 11175 Campus St Loma Linda CA 92350 USA;

    Loma Linda Univ Sch Dent Dent Res Ctr Chan Shun Pavil 11175 Campus St Loma Linda CA 92350 USA;

    Loma Linda Univ Sch Dent Dent Res Ctr Chan Shun Pavil 11175 Campus St Loma Linda CA 92350 USA;

    Loma Linda Univ Sch Dent Dent Res Ctr Chan Shun Pavil 11175 Campus St Loma Linda CA 92350 USA;

    Loma Linda Univ Sch Dent Res Loma Linda CA 92350 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 口腔科学;
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