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首页> 外文期刊>Clinical oral investigations >Randomized clinical trial of class II restoration in permanent teeth comparing ART with composite resin after 12 months
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Randomized clinical trial of class II restoration in permanent teeth comparing ART with composite resin after 12 months

机译:在12个月后将恒定牙齿恢复的随机临床试验恢复

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摘要

Objective This study evaluated the effectiveness of class II restorations, in permanent teeth, through the ART technique in comparison to composite resin. Materials and methods Participants (154), aged 8 to 19 years, with good general health, with class II cavities in permanent teeth, and without pulp involvement and tooth pain were included in this parallel and randomized clinical trial. The Ethics Committee approval number was CAAE: 24012913.0.1001.5417. Seventy-seven restorations were made with each restorative material (Equia Fil-GC Corporation and Z350-3M). Evaluations occurred at 6 and 12 months by the criteria of ART and the USPHS modified. Data were analyzed by Mann-Whitney, chi-square, Fisher's exact, chi-square tests with linear trend and logistic regression by enter method (p 0.050). Survival rates for restorations, regardless of the evaluation criteria used, are the same as the success rates, with the exception of ART restorations at 12 months of follow-up (94.8%). Conclusion No differences in the success rates of class II restorations of ART compared to resin composite, in permanent teeth, were observed after 12 months. Clinic significant HVGIC can safely be used to restore proximal cavities in permanent teeth up to 12 months.
机译:目的本研究评估了II型修复物,永久性牙齿的有效性,通过本领域的技术与复合树脂相比。材料和方法参与者(154),年龄8至19年,具有良好的一般健康,恒牙II类腔,没有纸浆受累和牙齿疼痛,包括在这种并行和随机临床试验中。道德委员会批准号是CAAE:24012913.0.1001.5417。使用每个恢复材料(Equia Fil-GC Corporation和Z350-3M)进行七十七种修复物。通过艺术标准和修改的USPH,评估发生在6和12个月。通过曼 - 惠特尼,费舍尔的精确,Chi-Square测试分析了数据,通过进入方法线性趋势和逻辑回归(P 0.050)。修复的生存率,无论使用的评估标准,与成功率相同,除了12个月的后续后的艺术修复物(94.8%)。结论12个月后,与恒牙相比,在恒定牙齿中,在恒定牙齿中没有常见艺术级修复率的成功率差异。临床显着的HVGIC可以安全地用于恢复长达12个月的永久性牙齿的近端腔。

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