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临床试验/NCT05497583
NCT05497583已完成不适用

Clinical Performance of Acetone Based HEMA-Free Universal Adhesive Versus Isopropanol Based HEMA-Free Universal Adhesive For Restoring Non-Carious Cervical Lesions Over A Period Of 18-Months Follow Up Using FDI Criteria: A Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2023年1月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
1
主要终点
Primary outcome (marginal staining)

研究概览

简要总结

because of the recent introduction of universal adhesives, little information is currently available about the bond durability of universal adhesives to various substrates. Evaluation of bond durability is important since the stability of the bond between the adhesive and substrates is related to the clinical success of restorations. Because significant hydrolysis of the dentin-resin interface occurs after 6-12 months, a clinical trial of at least 18 months' duration is indicated to more accurately depict the likelihood of long-term clinical success

详细描述

Cervical restorations are ever challenging because of difficulties in moisture control, caries access, and proximity to the gingival margin. Both mechanical and non-mechanical factors act to hinder the longevity of cervical restoration newer materials are readily introduced in the market with improved chemomechanical properties, longevity, patient safety, and comfort.

The introduction of new-generation adhesive systems has aimed at reducing technique sensitivity and the number of clinical steps required for adhesion. There has been a trend toward the use of less time-consuming options, continuing this trend, universal adhesives have recently been introduced to the profession. However, because of the recent introduction of universal adhesives, little information is currently available about the bond durability of universal adhesives to various substrates. Evaluation of bond durability is important since the stability of the bond between the adhesive and substrates is related to the clinical success of restorations. Although the most reliable conclusions about the performance of adhesives in the oral environment are derived from clinical trials.

To evaluate the effectiveness and clinical performance of adhesive systems, the American Dental Association (ADA) recommends clinical trials on non-carious cervical lesions (NCCLs), as composite resin restorations only remain bonded to these lesions by the micromechanical interlocking produced by the adhesive systems. The immediate, short-term, and long-term bonding performance of adhesive systems are then evaluated by retention, marginal integrity, and marginal discoloration. There are many attempts to improve bonding to substrates, bond strength, and bond durability, one of these attempts is the newly introduced universal adhesive (BeautiBond ).

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
Double (Participant, Outcomes Assessor)

盲法说明

double

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Participants had to be in good general health, be at least 18 years old
  • have an acceptable oral hygiene level
  • Participants were required to have NCCLs in different teeth preferably anterior or posterior that needed to be restored.
  • These lesions had to be noncarious
  • deeper than 1 mm
  • involve both the enamel and dentin of vital teeth without mobility.

排除标准

  • Uncooperative behavior, limits the use of adhesive due to hampering of adequate field or isolation techniques throughout the procedure.
  • Patients allergic to the adhesive material. Patients with extremely poor oral hygiene
  • severe or chronic periodontitis
  • heavy bruxism habits
  • Pulp involvement

研究组 & 干预措施

Acetone based HEMA free Universal Adhesive

Experimental

Patients with non-carious cervical lesions will be treated with Acetone Based HEMA-free Universal Adhesive (BeautiBond universal adhesive ) applied in a self-etch approach with (SE) selective enamel etching.

干预措施: Acetone based HEMA -free universal Adhesive (Other)

Isopropanol based HEMA-free universal Adhesive

Active Comparator

Patients with non-carious cervical lesions will be treated with isopropanol-based HEMA-free universal Adhesive (Prime&Bond universal™ Adhesive system) applied in a self-etch approach with (SE) selective enamel etching.

干预措施: Isopropanol based HEMA- free universal Adhesive (Other)

结局指标

主要结局

Primary outcome (marginal staining)

时间窗: 18 months

FDI (World Dental Federation)criteria

次要结局

  • Retention, marginal adaptation, Postoperative (Hyper-Sensitivity), and Recurrence of Caries(T0=Baseline immediate postoperative T1= 6 months follow up. T2=12 months follow up. T3=18 months follow up.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hanan Shawky Ramadan

principal investigator

Cairo University

研究点 (1)

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