Postoperative Pain Following the Use of the TruNatomy and XP-endo Shaper Systems: A Randomized Clinical Study

IF 3.6 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Journal of endodontics Pub Date : 2025-05-01 Epub Date: 2025-02-06 DOI:10.1016/j.joen.2025.01.022
Christianne Velozo PhD, Silmara Silva PhD, Wesley Viana MSc, Marina Isaltino MSc, Carolina Viana DDS, Pedro Freitas DDS, Diana Santana de Albuquerque PhD
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Abstract

Introduction

The present study aimed to clinically compare the incidence of postoperative pain after endodontic treatment of posterior teeth using XP-endo Shaper (XPES; FKG Dentaire, La Chaux-de-Fons, Switzerland) and TruNatomy (TNY; Dentsply Sirona, Ballaigues, Switzerland) systems.

Methods

In a single-blind randomized clinical trial, 104 vital teeth with an indication for conventional endodontic treatment for prosthetic purposes were treated by a single specialist following a pre-established protocol. All participants were unaware of the treatment they received. The teeth were randomly divided into 2 groups (n = 52) according to the instrumentation system used (TNY group and XPES group). The treatments were performed in a single visit. The participants were asked to rate the intensity of postoperative pain on a numeric rating scale and a visual analog scale (no pain, mild pain, moderate pain, and severe pain) after 24, 48, 72 h, and after 7 days.

Results

The incidence of postoperative pain was zero in both groups at 48 h, 72 h, and 7 days. At 24 h, most patients in the XPES and TNY groups had no pain, while the remaining participants in either group experienced mild pain (1–3), with no significant difference between groups (P > .05, Mann–Whitney test).

Conclusions

The instruments used in this study are associated with minimal postoperative pain, which only occurred in the first 24 h. Based on the parameters analyzed, we conclude that the systems tested cause mild postoperative pain over a short period of time.
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使用鼻切开术和XP-endo Shaper系统后的术后疼痛:一项随机临床研究。
前言:本研究旨在临床比较XP-endo Shaper (XPES;FKG Dentaire, La Chaux-de-Fons,瑞士)和TruNatomy (TNY;Dentsply Sirona, Ballaigues, Switzerland)系统。方法:在一项单盲随机临床试验中,由一名专家按照预先制定的方案治疗104颗具有常规牙髓治疗适应症的重要牙齿。所有的参与者都不知道他们所接受的治疗。根据使用的器械系统将牙随机分为2组(n = 52) (TNY组和XPES组)。治疗在一次访问中进行。参与者被要求在24、48、72小时和7天后用数字评定量表和视觉模拟量表(无疼痛、轻度疼痛、中度疼痛和重度疼痛)评定术后疼痛的强度。结果:两组患者术后48 h、72 h、7 d疼痛发生率均为零。24 h时,XPES组和TNY组大多数患者无疼痛,两组其余患者均有轻度疼痛(1 ~ 3),两组间差异无统计学意义(p < 0.05, Mann-Whitney检验)。结论:本研究中使用的器械与最小的术后疼痛相关,仅在前24小时内发生。根据分析的参数,我们得出结论,所测试的系统在短时间内引起轻度术后疼痛。
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 endodontics
Journal of endodontics 医学-牙科与口腔外科
CiteScore
8.80
自引率
9.50%
发文量
224
审稿时长
42 days
期刊介绍: The Journal of Endodontics, the official journal of the American Association of Endodontists, publishes scientific articles, case reports and comparison studies evaluating materials and methods of pulp conservation and endodontic treatment. Endodontists and general dentists can learn about new concepts in root canal treatment and the latest advances in techniques and instrumentation in the one journal that helps them keep pace with rapid changes in this field.
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