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临床试验/NCT05751382
NCT05751382终止不适用

3-year Evaluation of the Clinical Performances of a Self-adhesive Hybrid Resin Composite Compared to a Traditional Composite Resin Used for Direct Restorations of Non-carious Cervical Lesions (NCCLs): A Split-mouth Randomized Clinical Trial

Dentsply Sirona Implants and Consumables1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年9月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
16
试验地点
1
主要终点
Assessment of Restorative Quality

研究概览

简要总结

This is a split-mouth randomized clinical investigation conducted to evaluate clinical performances of a self-adhesive hybrid resin composite (investigational medical device Surefil) compared to a traditional composite resin, when used for direct restorations of non-carious lesions (NCCLs). The study consists of a 3-year long follow-up period.

详细描述

The aim of this study is to demonstrate non-inferiority in terms of clinical performance and patient discomfort after direct restorative treatment of class V NCCL with Surefil one restorative material (Dentsply Sirona) in combination with a traditional paste composite "Venus Pearl" employed in combination with iBond universal adhesive (Kulzer Dental) during an observational period of 3 years.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The aesthetic integration of the restoration will be evaluated by two experienced and blinded operators following the aesthetic criteria of the FDI.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients aging from 18 to 70
  • •40-60% women, 40-60% men
  • •Patients who present at least 2 cervical lesions on canines and / or upper premolars on vital teeth
  • •Patients who are not allergic or sensitive to the ingredients contained in the products
  • •The test patient consents to the restorative treatment in line with the study´s criteria (informed consent)
  • •Sufficiently understanding of the language

排除标准

  • •Extremely low level of oral hygiene
  • •Teeth with previous restorations
  • •Not possible adequate isolation of the operating area
  • •Patients with serious systemic diseases
  • •Devitalized teeth or with pulpitis in progress
  • •Periodontal problems on the elements to be restored

研究组 & 干预措施

Restoration with Surefil one hybrid composite

Experimental

In a split-mouth design, subjects were randomly assigned to restoration with Surefil one hybrid composite in either the left or the right upper quadrant.

Restoration performed with Surefil one hybrid composite applied according to manufacturer's instruction and cured for 20 seconds with a LED lamp (Smartlamp Pro).

干预措施: Surefil one (Device)

Restoration with Venus Pearl composite

Active Comparator

In a split-mouth design, subjects were randomly assigned to restoration with Venus Pearl composite in either the left or the right upper quadrant.

After the application of the adhesive system (iBond universal), the Venus Pearl composite will be layered on the cavity and cured for 20 seconds with a LED lamp Smartlamp Pro).

干预措施: Venus Pearl (Device)

结局指标

主要结局

Assessment of Restorative Quality

时间窗: At 36 months follow-up

The restorations will be evaluated using the United States Public Health Service (USPHS) criteria.

Assessment of Restorative Quality

时间窗: At 36 months follow-up.

The restorations will be evaluated using the World Dental Federation (FDI) criteria.

次要结局

  • Assessment of Restorative Quality(At 6, 12 and 24 months follow-up)
  • Level of Pain(At 6, 12, 24 and 36 months follow-up)
  • Assessment of Aesthetics(At 6, 12, 24 and 36 months follow-up)

研究者

发起方
Dentsply Sirona Implants and Consumables
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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