Comparison of the efficacy of aescin and diclofenac sodium in the management of postoperative sequelae and their effect on salivary Prostaglandin E2 and serum C-reactive protein levels after surgical removal of impacted mandibular third molar: a randomized, double-blind, controlled clinical trial.

Q2 Pharmacology, Toxicology and Pharmaceutics F1000Research Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.12688/f1000research.145643.3
Anuroop Singhai, Rajanikanth Kambala, Nitin Bhola
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Abstract

Introduction: Surgical removal of an impacted third molar is one of the most common oral surgical procedures performed in dental offices. The postoperative phase is often associated with severe inflammation. Non-steroidal anti-inflammatory drugs (NSAIDs) are usually prescribed to manage postoperative discomfort. NSAIDs have been associated with gastrointestinal bleeding, renal function disturbances, and platelet count reductions. Thus, the present study demonstrates the utility of aescin in managing postoperative discomfort after the surgical removal of impacted mandibular third molars.This study aimed to correlate and compare the impact of aescin and diclofenac on salivary PGE2 levels and serum C-reactive protein levels after surgical extraction of the mandibular third molar. The study will also evaluate and compare the effectiveness of individual drug therapy in managing postoperative pain, swelling and mouth opening.

Methods: The planned study is a single-center, double-blind, randomized, parallel, prospective clinical trial. Each patient will be prescribed either diclofenac sodium 150 mg/day or aescin (escin) 120 mg/day to be taken orally in divided doses for five days after surgically removing the impacted mandibular third molar.Pain will be assessed using a visual analog scale. Facial swelling and mouth opening will be recorded using a metric scale with standardized reference points. ELISA (enzyme-linked immunosorbent assay (ELISA) will be employed to measure salivary Prostaglandin E2 and serum C-reactive protein levels. All parameters will be recorded preoperatively (T0) on the second postoperative day (T1) and fifth postoperative day (T2).

Conclusion: The proposed study is expected to show a clinically acceptable response to the administration of aescin for the management of postoperative discomfort compared to diclofenac sodium after third molar surgery.The proposed study is expected to positively manipulate the levels of salivary Prostaglandin E2 and serum C-reactive protein, which are reliable inflammatory markers.The outcome of this study may provide an efficacious and safe alternative to conventional nonsteroidal anti-inflammatory drugs for managing postoperative discomfort following third molar surgery.

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比较阿司匹林和双氯芬酸钠治疗下颌第三磨牙撞击性手术后遗症的疗效及其对唾液前列腺素 E2 和血清 C 反应蛋白水平的影响:一项随机、双盲、对照临床试验。
介绍:手术切除撞击性第三磨牙是牙科诊所最常见的口腔外科手术之一。术后阶段往往伴有严重的炎症。非甾体类抗炎药(NSAIDs)通常用于控制术后不适。非甾体抗炎药与胃肠道出血、肾功能紊乱和血小板计数减少有关。因此,本研究证明了阿司匹林在手术拔除下颌第三磨牙后控制术后不适的作用。本研究旨在关联和比较阿司匹林和双氯芬酸对手术拔除下颌第三磨牙后唾液中 PGE2 水平和血清 C 反应蛋白水平的影响。该研究还将评估和比较个别药物疗法在控制术后疼痛、肿胀和张口方面的效果:计划中的研究是一项单中心、双盲、随机、平行、前瞻性临床试验。每位患者在手术切除下颌第三磨牙后,将被处方双氯芬酸钠 150 毫克/天或阿司匹林(escin)120 毫克/天,分次口服,连续五天。面部肿胀和张口情况将使用带有标准化参考点的量表进行记录。酶联免疫吸附试验(ELISA)将用于测量唾液前列腺素 E2 和血清 C 反应蛋白水平。所有参数将在术前(T0)、术后第二天(T1)和术后第五天(T2)进行记录:与双氯芬酸钠相比,拟进行的研究有望显示,在第三磨牙手术后使用阿司匹林治疗术后不适的反应可被临床接受。
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
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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