Clinica Odontoiatria Montesani, Rome, Italy.
LRM Statistical Consulting, West Orange, NJ, USA.
Clin Oral Investig. 2024 Jan 13;28(1):90. doi: 10.1007/s00784-023-05487-0.
To support the daily oral hygiene of patients experiencing gum inflammation, a new mouthwash was developed containing an amine + zinc lactate + fluoride system. In vitro and clinical efficacy was assessed using traditional methods as well as using novel site-specific and subject-specific analyses of the clinical data.
This mouthwash was evaluated in a 12-h biofilm regrowth assay against a negative control mouthwash and in a 6-month plaque and gingivitis clinical study as compared to a negative control mouthwash. Analyses of healthy versus inflamed sites, visible plaque versus non-visible plaque sites, as well as subject-level evaluations bring new perspectives to the overall performance of this mouthwash and its significance from a patient outcome perspective.
Studies demonstrated that this new mouthwash provided long-term (12-h) antibacterial activity after single application in vitro and reduced clinically all plaque and gingivitis parameters after 3 months and 6 months of use when compared to the negative control mouthwash. Examination of site-level and subject-level data determined that this mouthwash significantly increased the number of healthy sites in the oral cavity and significantly improved the gum health of subjects in the study, as compared to the negative control mouthwash.
In vitro and clinical research has demonstrated the antibacterial and clinical benefits of this mouthwash containing an amine compound + zinc lactate + fluoride system.
Our subject-specific and site-specific analyses provide the dental practitioner with tools that can be used to guide patients who suffer from gingivitis toward optimal product selection and use.
The trial was registered at ClinicalTrials.gov (reference no. NCT05821712).
为了支持患有牙龈炎的患者的日常口腔卫生,开发了一种含有胺+乳酸锌+氟化物系统的新型漱口液。使用传统方法以及对临床数据的新型特定部位和特定个体分析来评估其体外和临床疗效。
将该漱口液与阴性对照漱口液在 12 小时生物膜再生长试验中进行了评估,并与阴性对照漱口液在为期 6 个月的菌斑和牙龈炎临床研究中进行了比较。对健康部位与炎症部位、可见菌斑与不可见菌斑部位的分析,以及对个体水平的评估,为该漱口液的整体性能及其从患者结果角度的重要性带来了新的视角。
研究表明,该新型漱口液在体外单次应用后可提供长期(12 小时)抗菌活性,与阴性对照漱口液相比,在使用 3 个月和 6 个月后可显著降低所有菌斑和牙龈炎参数。对部位水平和个体水平数据的检查确定,与阴性对照漱口液相比,该漱口液可显著增加口腔内健康部位的数量,并显著改善研究中受试者的牙龈健康。
体外和临床研究证明了含有胺化合物+乳酸锌+氟化物系统的这种漱口液具有抗菌和临床益处。
我们的特定个体和特定部位分析为牙医提供了工具,可以用来指导患有牙龈炎的患者进行最佳产品选择和使用。
该试验在 ClinicalTrials.gov 上注册(参考编号:NCT05821712)。