Evaluation of the Anticaries Efficacy of Various Dentifrice Formulations Using an In-situ Model
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Mineral Density
研究概览
简要总结
The primary objective is to compare the remineralization and demineralization inhibition potential of early subsurface carious lesions in enamel in situ after rinsing with six different aqueous slurries of toothpaste formulations.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Be 18-75 years of age.
- •Provide written informed consent prior to participation and be given a signed copy of the informed consent form.
- •Be in good general health based on medical/dental history and oral exam.
- •Have no history of adverse or allergic reactions to tin or tin-containing products.
- •Agree not to participate in any other oral study for the study duration.
- •Have a reasonable functional dentition as determined by the oral examiner and sufficient teeth to support the fabricated dental appliance.
- •Be willing to participate in the study, able to follow the study directions, successfully tolerate/perform all study procedures, and willing to return for all specified visits at their appointed time.
- •Be willing to refrain from using non-study dentifrice, mouth rinse, chewing gum, and other non-study oral care products during the study.
- •Be willing to postpone all elective dental procedures until the study has been completed.
- •Be willing to refrain from using calcium chews while using the test products.
- •Be willing and able to refrain from wearing a nightguard (occlusal splint) for the entire course of the study (for nightguard wearers only).
- •Ability to understand, and ability to read and sign, the informed consent form.
- •Have at least 22 natural teeth.
- •Have a gum-stimulated whole salivary flow rate ≥ 1.0 ml/minute and unstimulated whole salivary flow rate ≥ 0.2 ml/minute.
排除标准
- 未提供
研究组 & 干预措施
Oral-B 1450 ppm Fluoride (1.16% sodium monofluorophosphate) Dentifrice
干预措施: Oral-B 1450 ppm Fluoride (1.16% sodium monofluorophosphate) Dentifrice (Drug)
Colgate 1450 ppm Fluoride (1.16% sodium monofluorophosphate)Dentifrice
干预措施: Colgate 1450 ppm Fluoride (1.16% sodium monofluorophosphate)Dentifrice (Drug)
Toms of Maine 0 ppm Fluoride Dentifrice
干预措施: Toms of Maine 0 ppm Fluoride Dentifrice (Drug)
Colgate 1450 ppm Fluoride (1.1% sodium monofluorophosphate) Dentifrice
干预措施: Colgate 1450 ppm Fluoride (1.1% sodium monofluorophosphate) Dentifrice (Drug)
1500 ppm MFP/CaCO3 1.16% sodium monofluorophosphate) Dentifrice
干预措施: 1500 ppm MFP/CaCO3 1.16% sodium monofluorophosphate) Dentifrice (Drug)
1100 ppm (0.454% Stannous fluoride) Dentifrice
干预措施: 1100 ppm (0.454% Stannous fluoride) Dentifrice (Drug)
结局指标
主要结局
Mineral Density
时间窗: 14 days
The percent mineral profile of each enamel/dentinel slab's demineralized control and remineralized/treated lesion, obtained from the microdensitometry analysis, will be compared with the median sound enamel percent mineral profile of the same section. A negative value indicates mineral has been lost and, therefore, the lesion has progressed, whereas a positive value indicates mineral has been gained and, therefore, the lesion has regressed.
Scanning Electron Microscopy (SEM)
时间窗: 14 days
SEM imaging and SEM-EDS analysis will be conducted on TMR sections and whole sections of dentine lesions treated in situ to assess the occlusion of dentine tubules and distribution of elements within the lesions following the experiment.
次要结局
未报告次要终点