Schenke Isabelle M, Pfister Julia L, Hiller Karl-Anton, Buchalla Wolfgang, Cieplik Fabian, Ettenberger Sarah, Scholz Konstantin J, Federlin Marianne
Department of Conservative Dentistry and Periodontology, University Hospital Regensburg, Germany.
Department of Conservative Dentistry and Periodontology, University Hospital Regensburg, Germany.
J Dent. 2025 May;156:105663. doi: 10.1016/j.jdent.2025.105663. Epub 2025 Mar 17.
In this randomized prospective split-mouth study, the clinical survival and performance of a novel not yet commercially available self-adhesive dual-curing bulk-fill restorative material (SA, Solventum) and a conventional bulk-fill composite (Filtek One, Solventum; FO) were examined for restoration of class II cavities over a period of 60 months.
30 patients underwent the placement of one SA and one FO restoration each. FO restorations were bonded using Scotchbond Universal (Solventum) in self-etch mode, while SA was applied without adhesive. This publication reports restoration survival as a primary outcome and quality parameters of restorations according to FDI criteria as a secondary outcome at baseline, 48 and 60 months. Restorations were evaluated by two independent examiners. Kaplan-Meier survival analysis and non-parametric statistical methods were employed (χ-tests; α=0.05).The study was registered prior to commencement (German Register of Clinical Studies: DRKS00013564).
25 patients out of initially 30 were available at 60-mo recall. At 60-mo, FO exhibited a clinical survival rate of 97.1 % and SA of 98.9 % without significant difference (p > 0.05). All restorations available for clinical evaluation maintained clinically acceptable FDI scores throughout the follow-up period. FO significantly outperformed SA in terms of surface luster, color match and translucency at both evaluation time points, in terms of marginal staining at 60-mo and in terms of surface staining at 48-mo. Surface luster, surface staining and marginal adaptation deteriorated over time for both materials.
Both materials demonstrated similar clinical survival and performance over 60 months, which is to date the longest observation period for a clinical study including a self-adhesive bulk-fill restorative. SA displayed slightly inferior but clinically acceptable esthetic properties compared to FO. Both materials exhibited clinically acceptable outcomes over 60 months, warranting their recommendation for clinical use.
The novel self-adhesive dual-curing bulk-fill restorative material exhibited clinically acceptable outcomes over 60 months, similarly to a conventional bulk-fill restorative used with a universal adhesive, with only minor cutbacks in esthetic properties. Thus, both materials can be considered suitable for clinical application.
在这项随机前瞻性半口研究中,对一种新型的尚未上市的自粘性双固化大块充填修复材料(SA,Solventum)和一种传统的大块充填复合材料(Filtek One,Solventum;FO)在60个月期间修复Ⅱ类洞的临床存留率和性能进行了研究。
30例患者分别接受了一个SA修复体和一个FO修复体的放置。FO修复体采用Scotchbond Universal(Solventum)自酸蚀模式粘结,而SA修复体未使用粘结剂。本研究报告了修复体存留率作为主要结局,以及根据FDI标准评估的修复体质量参数作为次要结局,分别在基线、48个月和60个月时进行评估。修复体由两名独立的检查者进行评估。采用Kaplan-Meier生存分析和非参数统计方法(χ检验;α=0.05)。该研究在开始前已注册(德国临床研究注册:DRKS00013564)。
最初的30例患者中有25例在60个月随访时仍可进行评估。在60个月时,FO的临床存留率为97.1%,SA为98.9%,两者无显著差异(p>0.05)。所有可供临床评估的修复体在整个随访期间均保持了临床可接受的FDI评分。在两个评估时间点,FO在表面光泽、颜色匹配和透明度方面均显著优于SA,在60个月时的边缘染色方面以及在48个月时的表面染色方面也优于SA。两种材料的表面光泽、表面染色和边缘适应性均随时间恶化。
两种材料在60个月内均表现出相似的临床存留率和性能,这是迄今为止包括自粘性大块充填修复体在内的临床研究最长的观察期。与FO相比,SA的美学性能略差,但仍在临床可接受范围内。两种材料在60个月内均表现出临床可接受的结果,因此推荐临床使用。
这种新型的自粘性双固化大块充填修复材料在60个月内表现出临床可接受的结果,与使用通用粘结剂的传统大块充填修复材料相似,只是美学性能略有下降。因此,两种材料都可被认为适合临床应用。