24- Month Clinical Performance of Injectable and Conventional Resin Composites in Class I Cavities

Hacettepe University2 个研究点分布在 1 个国家目标入组 30 人开始时间: 2023年6月12日最近更新: 2025年11月18日

适应症

试验速览

阶段: 不适用
状态: 进行中（未招募）
发起方: Hacettepe University
入组人数: 30
试验地点: 2
主要终点: Marginal Adaptation

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Purpose of research: Evaluation and comparison of 24-month clinical performance of injectable and conventional resin composites in class I cavities.

详细描述

The mechanical properties of conventional resin composites have been tried to be improved. In addition to the developed mechanical properties, the need for easy and fast application led to the development of flowable composites. Flowable composites have lower filler ratio than conventional hybrid composites so they are less rigid and have lower modulus of elasticity. For these reasons, the use of flowable composites in areas that may be exposed to high forces, especially occlusal cavities, is not recommended. Today, it is aimed to increase the wear resistance by increasing the amount of filler in flowable composites and producing injectable composites. A new product recently introduced to the market, a high-strength nano-filled injectable composite material, GC's G-ænial Universal Injectable(Tokyo,Japan), was also included in the study. This is a low-viscosity composite in which modifications have been made to provide a product with high wear resistance and depth of cure to make it suitable for posterior restorations.

One lesion in each patient will be randomly assigned to be restored using either the G-aenial Universal Injectable or Filtek Z250 resin composites. The adhesive, G2-BOND Universal will be used for adhesive procedures. The clinical procedure for the restorations will be performed by a single operator. The restorations will be evaluated by two calibrated examiners at baseline and at 6, 12, 18, 24 months in accordance with the modified USPHS criteria. Data will be statistically analyzed using the Chi-square and Cochran Q tests (p < 0.05).

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: Single (Participant)

入排标准

年龄范围: 18 Years 至 35 Years（Adult）
性别: All
接受健康志愿者: 是

入选标准

•Healthy individuals who do not have any systemic disease that prevents restorative treatment
•Individuals between the ages of 18-35
•Brushing your teeth twice a day
•Having at least 20 teeth in occlusion and at least 2 occlusal lesions with antagonist teeth in the opposite arch
•Volunteer individuals who agree to participate in the research and sign the informed consent form and who have undergone initial periodontal treatment will be included in the study.

排除标准

•Pregnant or breastfeeding women
•Individuals with advanced periodontal disease
•Individuals using removable partial dentures
•Individuals with bruxism
•Individuals with malocclusion
•Patients with known allergies to resin-based restorative materials and bonding agents
•Patients with a history of allergy to local anesthesia
•Endodontic treatment, teeth that need pulp capping or endodontic treatment is available