Assessing the influence of Katana™ Cleaner on the clinical performance of bulk-fill restorations in endodontically treated teeth: study protocol for a randomized clinical study.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-05-07 DOI:10.1186/s13063-025-08790-1
Jacqueline Vitória do Nascimento Azevedo, Ceci Nunes Carvalho, Hadda Lyzandra Austriaco Leite, Suellen Nogueira Linares Lima, Wallace Vieira Mendes, Sebastião Marinho Pinheiro Neto, Andrés Felipe Millian Cardenas, Fabiana Suellen Figueredo Siqueira, Rossana Aboud Matos de Almeida, Etevaldo Matos Maia Filho
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引用次数: 0

Abstract

Background: Complete cleaning of the pulp chamber interior is a mandatory step before the restorative process. Ethanol is the most commonly used substance for cleaning the dentin surface; however, studies report that ethanol is ineffective at completely removing residues. Although Katana™ is recommended for prosthetic purposes, in vitro studies have shown it delivers results equal to or better than ethanol. The study aims to evaluate the influence of Katana™ Cleaner on cleaning the pulp chamber of teeth treated endodontically with an epoxy or bioceramic sealer and on the clinical performance of bulk-fill resin restorations over an 18-month follow-up period, using two clinical performance criteria: World Dental Federation (FDI) and United States Public Health Service (USPHS).

Methods: The study will be a blinded randomized clinical trial conducted according to the Consolidated Standards of Reporting Trials (CONSORT) statement. Selected patients (n = 224) will undergo pulp chamber cleaning following endodontic obturation with epoxy and bioceramic sealers, divided into four treatment groups (Katana and AH Plus, Katana and Bioceramic, Ethanol and AH Plus, Ethanol and Bioceramic), followed by bulk-fill resin restorations. The clinical performance of the restorations will be evaluated at the following intervals: 1 week, 3, 6, 9, 12, 15, and 18 months, using two evaluation criteria: FDI and USPHS. Results will be analyzed using survival analysis with the Kaplan-Meier estimator to assess failure occurrence over time for the two treatments. A Cox regression analysis will be conducted to evaluate the risk of failure. A 5% significance level will be adopted for all tests.

Discussion: The proposed study will be the first to examine the clinical effects of a new cleaning protocol on the removal of endodontic sealer residues. We will also explore potential improvements that Katana may provide in the bond strength of a self-etch adhesive to dentin in teeth restored with composite resin. If promising results are observed in clinical trials, this would suggest that individuals could benefit from the intervention using the proposed protocol, highlighting the potential for improved outcomes in the restorations of endodontically treated teeth. Additionally, it could pave the way for future studies in this field.

Trial registration: Registered in the Brazilian Registry of Clinical Trials (REBEC: RBR-86ycwq7) on February 29, 2024.

评估Katana™Cleaner对根管治疗牙体填充修复体临床性能的影响:随机临床研究的研究方案
背景:彻底清洁牙髓腔内部是修复过程前的必要步骤。乙醇是清洁牙本质表面最常用的物质;然而,研究报告说,乙醇在完全去除残留物方面是无效的。虽然Katana™被推荐用于假体用途,但体外研究表明,它提供的结果等于或优于乙醇。本研究旨在评估Katana™Cleaner在用环氧树脂或生物陶瓷密封剂进行根管治疗的牙齿的牙髓腔清洁方面的影响,以及在18个月的随访期内,使用两个临床性能标准:世界牙科联合会(FDI)和美国公共卫生服务(USPHS)。方法:该研究将是一项盲法随机临床试验,根据联合报告试验标准(CONSORT)声明进行。选择的患者(n = 224)在根管封闭后使用环氧树脂和生物陶瓷密封剂进行牙髓腔清洁,分为4个治疗组(Katana和AH Plus、Katana和生物陶瓷、乙醇和AH Plus、乙醇和生物陶瓷),然后进行体填充树脂修复。采用FDI和USPHS两项评估标准,对修复体的临床表现进行评估,评估时间间隔为:1周、3、6、9、12、15和18个月。结果将使用Kaplan-Meier估计器进行生存分析,以评估两种治疗随时间的失败发生率。采用Cox回归分析对失效风险进行评估。所有测试采用5%的显著性水平。讨论:提出的研究将是第一个检查一种新的清洁方案对去除根管密封残留物的临床效果。我们也将探索潜在的改进,武士刀可能提供自蚀刻粘合剂与牙本质的结合强度与复合树脂修复的牙齿。如果在临床试验中观察到有希望的结果,这将表明个人可以从使用提议的方案的干预中受益,突出了在髓内治疗的牙齿修复中改善结果的潜力。此外,它可以为该领域的未来研究铺平道路。试验注册:于2024年2月29日在巴西临床试验注册中心(REBEC: RBR-86ycwq7)注册。
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
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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