Assessment of coated orthodontic miniscrews with chlorhexidine hexametaphosphate antimicrobial nanoparticles: A randomized clinical trial.

IF 2.6 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Ahmed Ali Al-Hilaly, Akram Faisal Alhuwaizi
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引用次数: 0

Abstract

Background: Using miniscrews to control anchorage made the application of force for various orthodontic treatment approaches easier and increased their effectiveness. Some problems may occur during the use of miniscrews, such as peri‑implant mucositis, mobility, postoperative pain, and failure. This study compared the success rate of miniscrews coated with chlorhexidine hexametaphosphate antimicrobial nanoparticles with that of uncoated miniscrews.

Methods: In a double-blind randomized controlled clinical trial using a split-mouth design, 80 miniscrews were inserted symmetrically into 40 individuals between the maxillary second premolar and first molar. Random allocation software was used to distribute the coated and uncoated miniscrews. The patients were monitored monthly, for a duration of 4 months. The main measure of interest was the success rate of miniscrews, which was assessed throughout follow-up periods of up to 4 months. The secondary objective was the assessment of the mobility of the miniscrews, peri‑implant health, and pain perception. A Wilcoxon signed-rank test and Kaplan-Meier survival analysis were applied to analyze the data.

Results: Main outcome: After the 4-month follow-up, the success rates of the miniscrews for coated and uncoated samples were 81.3% and 84.4%, respectively, which was a statistically insignificant difference.

Secondary outcome: Mobility and peri‑implant health were not statistically different between the coated and uncoated miniscrew groups. Pain intensity was rated higher on the first day, then decreased gradually, diminishing completely on the sixth and seventh day. However, the pain perception between the coated and uncoated miniscrews did not differ statistically.

Conclusions: Chlorhexidine-hexametaphosphate nanoparticles did not increase the success rate and stability, nor did they enhance peri‑implant health or affect pain perception during the short observation period.

Trial registration: This trial was registered at ClinicalTrials.gov; ID: NCT06124235.

评估涂有六偏磷酸钠洗必泰抗菌纳米粒子的正畸微型螺丝:随机临床试验。
背景:使用微型螺钉控制锚固使各种正畸治疗方法的施力变得更容易,并提高了治疗效果。使用微型螺丝时可能会出现一些问题,如种植体周围粘膜炎、移动性、术后疼痛和失败。本研究比较了涂有洗必泰六偏磷酸钠抗菌纳米颗粒的微型螺钉与未涂药微型螺钉的成功率:在一项双盲随机对照临床试验中,采用分口设计,将 80 个迷你螺钉对称插入 40 名患者的上颌第二前磨牙和第一磨牙之间。使用随机分配软件来分配有涂层和无涂层的微型螺钉。在为期 4 个月的时间里,每月对患者进行监测。主要指标是微型螺钉的成功率,在长达 4 个月的随访期间进行评估。次要目标是评估微型螺钉的活动度、种植体周围健康状况和疼痛感。数据分析采用 Wilcoxon 符号秩检验和 Kaplan-Meier 生存分析:主要结果4个月随访后,有涂层和无涂层样本的微型螺丝成功率分别为81.3%和84.4%,差异无统计学意义:有涂层和无涂层迷你螺钉组的活动度和种植体周围健康状况无统计学差异。第一天的疼痛强度较高,然后逐渐降低,在第六天和第七天完全减轻。然而,有涂层和无涂层迷你螺钉之间的疼痛感没有统计学差异:结论:在短时间的观察期内,氯己定-六偏磷酸钠纳米粒子并没有提高成功率和稳定性,也没有增强种植体周围的健康或影响疼痛感:该试验已在 ClinicalTrials.gov 注册;ID:NCT06124235。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the World Federation of Orthodontists
Journal of the World Federation of Orthodontists DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.80
自引率
4.80%
发文量
34
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