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一种含有壳聚糖、洗必泰、尿囊素和泛醇的局部凝胶在第三磨牙手术后控制疼痛和炎症的疗效:一项随机安慰剂对照临床试验。

Efficacy of a topical gel containing chitosan, chlorhexidine, allantoin and dexpanthenol for pain and inflammation control after third molar surgery: A randomized and placebo-controlled clinical trial.

出版信息

Med Oral Patol Oral Cir Bucal. 2020 Sep 1;25(5):e644-e651. doi: 10.4317/medoral.23661.

Abstract

BACKGROUND

The aim of this study was to evaluate and compare the postoperative effect of a topic gel containing chlorhexidine, chitosan, allantoine and dexpanthenol versus a placebo for pain and inflammation control after third molar surgery.

MATERIAL AND METHODS

A gel combining 0.2% chlorhexdine, 0.5% chitosan, 5% dexpanthenol, 0.15% allantoin and 0.01% sodium saccharin was selected for this split mouth randomized controlled and double-blind trial including 36 patients with bilaterally and symmetrically impacted lower third molars. The teeth (n=72) were randomly divided into two groups before surgical removal: control group (CG; in which a placebo was given) and experimental group (EG). Swelling, trismus, postoperative pain, wound healing and complications were measured and recorded in order to evaluate differences between the placebo and experimental product.

RESULTS

Five patients suffered from an alveolitis in the CG (13.9%), and none in the study group (0%), but no statistically significant difference was found (p=0.063). From day 0 to day 7, trismus and swelling were significantly less pronounced in the EG, and wound healing was considered 'good' in 22.2% for the CG and 97.2% for the EG (p<0.001). Mean VAS scores during the seven postoperative days were statistically lower in the study (2.56±1,19) compared to the placebo group (3.25±1.6) (p=0.002). The mean consumption of analgesic pills during the first 92 hours was also statistically lower in the EG (0.26±0.51) in comparison to the CG (0.56±0.67) (p=0.003).

CONCLUSIONS

The use of an experimental gel containing chlorhexidine, chitosan, allantoine and dexpanthenol seems to significantly reduce postoperative pain, trismus and signs of inflammation. Future studies should further evaluate, if the gel is effective in dry socket preventing after third molar removal.

摘要

背景

本研究旨在评估和比较一种含有洗必泰、壳聚糖、尿囊素和泛醇的主题凝胶与安慰剂在第三磨牙手术后控制疼痛和炎症的术后效果。

材料和方法

选择一种含有 0.2%洗必泰、0.5%壳聚糖、5%泛醇、0.15%尿囊素和 0.01%蔗糖素的凝胶进行这项随机对照、双盲、劈裂口腔试验,纳入 36 名双侧和对称阻生的下颌第三磨牙患者。在手术切除前,将牙齿(n=72)随机分为两组:对照组(CG;给予安慰剂)和实验组(EG)。为了评估安慰剂和实验产品之间的差异,测量并记录肿胀、牙关紧闭、术后疼痛、伤口愈合和并发症。

结果

CG 中有 5 名患者(13.9%)发生牙槽炎,而研究组中没有(0%),但无统计学显著差异(p=0.063)。从第 0 天到第 7 天,EG 中的牙关紧闭和肿胀明显减轻,CG 中的愈合情况被认为是“良好”的为 22.2%,而 EG 中的愈合情况为 97.2%(p<0.001)。在术后 7 天内,研究组的平均 VAS 评分(2.56±1.19)明显低于安慰剂组(3.25±1.6)(p=0.002)。在头 92 小时内,EG 中镇痛药的平均消耗量(0.26±0.51)也明显低于 CG(0.56±0.67)(p=0.003)。

结论

使用含有洗必泰、壳聚糖、尿囊素和泛醇的实验凝胶似乎可以显著减轻术后疼痛、牙关紧闭和炎症迹象。未来的研究应进一步评估该凝胶在预防第三磨牙拔除后干槽症方面的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/299a/7473436/2c1b2071f30a/medoral-25-e644-g001.jpg

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