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两种美白牙膏的牙齿美白及外源性牙渍清除效果比较:六周临床试验

Comparative tooth whitening and extrinsic tooth stain removal efficacy of two tooth whitening dentifrices: six-week clinical trial.

作者信息

Soparkar Pramod, Rustogi Kedar, Zhang Yun Po, Petrone Margaret E, DeVizio William, Proskin Howard M

机构信息

Harrisburg Clinical Dental Research Center, Grantville, PA, USA.

出版信息

J Clin Dent. 2004;15(2):46-51.

Abstract

OBJECTIVE

The objective of this six-week, examiner-blind clinical study was to assess the tooth whitening and extrinsic tooth stain removal efficacy of a new dentifrice delivering 1.0% hydrogen peroxide, 0.243% sodium fluoride, and sodium tripolyphosphate in a high-cleaning silica base (Test Dentifrice), relative to that of commercially available hexametaphosphate-containing whitening dentifrice (Positive Control Dentifrice).

METHODOLOGY

Following a baseline oral soft tissue examination and scoring of extrinsic tooth stain and tooth shade, qualifying adult male and female subjects from the Harrisburg, Pennsylvania area were randomized into either the Test or Positive Control Dentifrice group. The two groups were balanced for gender, extrinsic tooth stain, and tooth shade scores. All subjects were provided their assigned dentifrice and a soft-bristled adult toothbrush for home use. Subjects were instructed to brush their teeth for two minutes twice daily (morning and evening) using only the dentifrice provided, and to refrain from using any other oral hygiene products for the entire six weeks of the study. There were no restrictions regarding diet or smoking habits during the course of the study. Oral soft tissue, extrinsic tooth stain, and tooth shade assessments for each subject were repeated after two and six weeks of product use. All statistical tests were two sided and employed a level of significance of alpha = 0.05.

RESULTS

Fifty-six (56) subjects complied with the protocol and completed the entire study. Compared to baseline at both the two- and six-week examinations, the Test Dentifrice group had statistically significant reductions in extrinsic tooth stain area and intensity, and statistically significant mean shade rank reductions, with a six-week reduction of 4.81. In contrast, at six weeks, the Positive Control dentifrice had a statistically significant increase in tooth stain area, a non-significant increase in tooth stain intensity, and a statistically significant mean 1.40 shade rank score reduction. At both the two- and six-week examinations, the Test Dentifrice group had statistically significantly lighter tooth shades and statistically significantly lower levels of extrinsic tooth stain area and intensity than the Positive Control Dentifrice group.

CONCLUSION

A new whitening dentifrice delivering 1.0% hydrogen peroxide, 0.243% sodium fluoride, and sodium tripolyphosphate in a high-cleaning silica base has significant efficacy in tooth whitening and extrinsic stain removal, and provides a statistically significantly greater level of efficacy for both tooth whitening and extrinsic tooth stain removal than the commercially available Positive Control Dentifrice.

摘要

目的

这项为期六周的、检查者盲法临床研究的目的是评估一种新型牙膏的牙齿美白和去除外源性牙渍的效果。该牙膏含有1.0%的过氧化氢、0.243%的氟化钠和三聚磷酸钠,以高清洁度的二氧化硅为基质(测试牙膏),并与市售的含六偏磷酸钠的美白牙膏(阳性对照牙膏)进行比较。

方法

在进行基线口腔软组织检查以及对外源性牙渍和牙齿色泽进行评分之后,来自宾夕法尼亚州哈里斯堡地区符合条件的成年男性和女性受试者被随机分为测试牙膏组或阳性对照牙膏组。两组在性别、外源性牙渍和牙齿色泽评分方面保持平衡。为所有受试者提供了他们所分配的牙膏和一支软毛成人牙刷供家庭使用。受试者被指示每天早晚仅使用所提供的牙膏刷牙两分钟,并在研究的整个六周内避免使用任何其他口腔卫生产品。在研究过程中,对饮食或吸烟习惯没有限制。在使用产品两周和六周后,对每个受试者的口腔软组织、外源性牙渍和牙齿色泽进行重新评估。所有统计检验均为双侧检验,显著性水平为α = 0.05。

结果

五十六(56)名受试者遵守了方案并完成了整个研究。与两周和六周检查时的基线相比,测试牙膏组在外源性牙渍面积和强度方面有统计学显著降低,在平均色泽等级方面也有统计学显著降低,六周时降低了4.81。相比之下,在六周时,阳性对照牙膏的牙渍面积有统计学显著增加,牙渍强度有不显著增加,平均色泽等级得分有统计学显著降低1.40。在两周和六周检查时,测试牙膏组的牙齿色泽比阳性对照牙膏组显著更浅,外源性牙渍面积和强度水平也显著更低。

结论

一种新型美白牙膏,含有1.0%的过氧化氢、0.243%的氟化钠和三聚磷酸钠,以高清洁度的二氧化硅为基质,在牙齿美白和去除外源性污渍方面具有显著效果,并且在牙齿美白和去除外源性牙渍方面提供了比市售阳性对照牙膏在统计学上显著更高的功效水平。

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