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首页> 外文期刊>BMC Complementary and Alternative Medicine >Evaluation of Salvadora persica L. and green tea anti-plaque effect: a randomized controlled crossover clinical trial
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Evaluation of Salvadora persica L. and green tea anti-plaque effect: a randomized controlled crossover clinical trial

机译:Salvadora persica L.和绿茶抗牙菌斑作用的评估:随机对照交叉临床试验

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Background In the author’s earlier in vitro investigation, a combination of 0.25?mg/ml green tea and 7.82?mg/ml Salvadora persica L. aqueous extracts was found to exhibit significant synergistic anti-bacterial and anti-adherence effects against primary plaque colonizers biofilm. A clinical trial was needed to support these preliminary in vitro results and to investigate its efficacy as a mouthwash in the control of dental plaque. Methods A 24?h plaque re-growth, double-blinded, randomized crossover trial was carried out. Participants (n?=?14) randomly rinsed with test formulation, 0.12% chlorhexidine (control) and placebo mouthwashes for 24?h. A week before the trial, all participants received scaling, polishing and oral hygiene education. On the trial day, the participants received polishing at baseline and rinsed with 15?ml of randomly allocated mouthwash twice daily without oral hygiene measures. After 24?h, plaque index was scored and then the participants entered a 6-days washout period with regular oral hygiene measures. The same protocol was repeated for the next 2 mouthwashes. Results The results were expressed as mean (±SD) plaque index. The test mouthwash (0.931?±?0.372) significantly reduced plaque accumulation when compared with placebo (1.440?±?0.498, p 0.0167). Conclusions The test mouthwash has an anti-plaque effect for a 24?h period. Longer-term clinical studies are highly encouraged to investigate its anti-plaque effect for longer periods. Trial registration This study was registered in ClinicalTrials.gov as NCT02624336 in December 3, 2015.
机译:背景技术在作者较早的体外研究中,发现0.25?mg / ml绿茶和7.82?mg / ml Salvadora persica L.水提物的组合对主要菌斑定殖剂生物膜具有显着的协同抗菌和抗粘附作用。 。需要临床试验来支持这些初步的体外结果,并研究其作为漱口水在控制牙菌斑中的功效。方法进行了24小时噬菌斑重生,双盲,随机交叉试验。用试验配方,0.12%洗必太(对照)和安慰剂漱口水将参与者(n≥14)随机冲洗24小时。试验前一周,所有参与者均接受了洗牙,上光和口腔卫生教育。在试验的当天,参与者在基线时进行了抛光,并每天用15毫升的随机分配的漱口水冲洗两次,无需口腔卫生措施。 24小时后,对牙菌斑指数进行评分,然后参与者通过常规口腔卫生措施进入6天的清除期。接下来的两次漱口水重复相同的步骤。结果结果表示为平均(±SD)菌斑指数。与安慰剂相比(1.440±±0.498,p 0.0167),试验漱口水(0.931±±0.372)显着减少了斑块积聚。结论测试的漱口水具有24小时的抗牙菌斑作用。强烈建议进行长期临床研究,以更长时间地研究其抗牙菌斑的作用。试验注册该研究于2015年12月3日在ClinicalTrials.gov中注册为NCT02624336。

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