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临床试验/NCT03624894
NCT03624894Unknown不适用

Suitability of Intraoral Impressions for Assessment of Wear of Teeth and Restorative Materials Over 60 Months Using the Replica Method and 3-D Laser Equipment.

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio0 个研究点目标入组 33 人开始时间: 2016年2月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
33
主要终点
Wear of teeth and materials of restorations

研究概览

简要总结

Suitability of intraoral impressions for assessment of wear of teeth and restorative materials over 60 months, using the gypsum replica method and 3-D laser scanning: perspective clinical and laboratory evaluation.

详细描述

The study will assess suitability of intraoral impressions for assessment of wear of artificial dental restorative materials over 60 months. Subjects are recruit from patients that undergo a dental restorations independently from the present study. The sample size of n=65 would enable detection of differences in material and tooth wear greater than 10-13% from the baseline volume of teeth, when compared with volumes of teeth obtained from impressions taken at follow-ups, with the power of 0.8 and for the significance level of p=0.05. Paired t-test or a Wilcoxon signed-rank test is implemented depending on the distribution of the variables, for primary aim of evaluating suitability of polyvinylsiloxane dental impression for determination of wearing of teeth and restorative materials.

Paired t-test for each sub-score or a Wilcoxon-signed rank test is implemented, depending on the distribution of the variables, for secondary aims. Then, if variables are considered also as categorical, a Mc Nemar test for each sub-score will be suggested

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subject ≥18 years.
  • Subjects with restorative treatments on vital teeth in posterior molar region. Will be considered at most one reconstruction per side.
  • Restorations limited to two surfaces (Black's Class II) with one proximal cavity, in occlusion. Max 1 restoration will be included each oral side (right or left).
  • Favorable and stable occlusal relationship between the remaining teeth.
  • Subject must be reliable, cooperative, and in the opinion of the Investigator, likely to be compliant with study procedures.
  • Subject provides written informed consent signed and dated prior to entering the study.

排除标准

  • Inclusion and exclusion criteria
  • Inclusion criteria
  • Subject ≥18 years.
  • Subjects with restorative treatments on vital teeth in posterior molar region. Will be considered at most one reconstruction per side.
  • Restorations limited to two surfaces (Black's Class II) with one proximal cavity, in occlusion. Max 1 restoration will be included each oral side (right or left).
  • Favorable and stable occlusal relationship between the remaining teeth.
  • Subject must be reliable, cooperative, and in the opinion of the Investigator, likely to be compliant with study procedures.
  • Subject provides written informed consent signed and dated prior to entering the study.
  • Exclusion criteria
  • Subject with full dentures or crowns and bridges in occlusal contact with teeth indicated for restorative treatment.
  • Absence of occlusal contact.
  • Subject has a history of drug abuse, addiction to medication or alcohol abuse within the previous year.
  • Pulp exposure during restorative procedure or unvital teeth.
  • Known unavailability of subject for recall Visit(s).
  • Allergy to any ingredient of impression material.
  • Severe bruxism.
  • Subject with clinically significant or unstable medical or physiological condition.
  • Female subject is pregnant or lactating or intends to become pregnant during the course of the study.
  • Subject is not willing to participate in the study or not able to understand the content of the study

结局指标

主要结局

Wear of teeth and materials of restorations

时间窗: 5 years

3D models will be obtained from intraoral impressions taken at baseline, at 3 and at 5 years fo follow-up. 3D models obtained at different times will be compared by a 3D software (Aadva LabScan Software, GC Corporation, Japan), able to overlap the volumes and identify all areas where surfaces have been worn. The software is able to create graphical images of the occurred wear, but also to numerically quantify the volume lost due to wear. The software is able to evaluate differences till 0,001 mm, but for this study the limit for precision had been set to 0,01 mm.

次要结局

  • Level of wear of different restorative materials(5 years)

研究者

发起方
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
申办方类型
Other
责任方
Sponsor

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