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A 1-year appraisal of pit and fissure sealants following disinfection with and without chlorhexidine solution: An in vivo randomized trial

机译:对有和没有洗必泰溶液消毒后的窝沟密封剂进行为期1年的评估:一项体内随机试验

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Objective: The objective of this study is to evaluate the effect of chlorhexidine on the outcome of pit and fissure sealant (PFS) in permanent molars. Methods: A double-blind randomized controlled trial using split-mouth design was conducted for a period of 1 year. The clinical trial registry was done in the Indian Council of Medical Research, and the clinical trial number obtained was CTRI/2016/08/007222. The age group of participants involved in the trial was 7–14 years. Maxillary or mandibular permanent molar which satisfies the criteria for application of PFS was included in the trial. Based on the eligibility criteria and considering the unknown observer/instrumentation errors, the sample size is 33 for each group. Simple randomization of treatment allocation was carried out using computer-generated random number for treatment assignment of the right molar tooth. The left molar received the alternative treatment. The outcomes of PFS were evaluated by a lone proficient assessor by means of the mouth mirrors and probes following the US public health service criteria. Results: A 6-month evaluation for the PFS with and without chlorhexidine showed 77.27% and 89.39% retention, respectively. PFS without chlorhexidine suffered a greater loss of surface texture and marginal discoloration in comparison to PFS with chlorhexidine at 3-, 6-, and 12-month intervals, but it was statistically insignificant. Conclusion: The present study showed improvement in outcome of PFS when an additional step of chlorhexidine is added although the results were statistically nonsignificant.
机译:目的:本研究的目的是评估洗必泰对恒磨牙中凹坑和裂隙封闭剂(PFS)结局的影响。方法:采用裂口设计的双盲随机对照试验进行了1年。临床试验注册在印度医学研究理事会进行,获得的临床试验编号为CTRI / 2016/08/007222。参与试验的参与者年龄组是7-14岁。符合PFS应用标准的上颌或下颌恒磨牙被纳入试验。根据资格标准并考虑未知的观察者/仪器错误,每组样本量为33。使用计算机生成的随机数对右臼齿进行简单的治疗分配随机化。左磨牙接受替代治疗。根据美国公共卫生服务标准,由一名熟练的评估员通过口镜和探头对PFS的结果进行评估。结果:有和没有洗必泰的PFS的6个月评估显示保留率分别为77.27%和89.39%。与使用洗必泰的PFS在3、6和12个月的时间间隔相比,没有洗必泰的PFS遭受更大的表面质感损失和边缘变色,但在统计学上不显着。结论:本研究显示,当增加洗必太步骤时,PFS的预后得到改善,尽管结果在统计学上无统计学意义。

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