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临床试验/NCT07691658
NCT07691658进行中(未招募)不适用

Clinical Evaluation of Prefabricated Versus 3D-Printed Composite Resin Veneers: in Vivo Study

Tanta University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年4月25日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40
试验地点
1
主要终点
Color match and stability

研究概览

简要总结

The purpose of this study is to clinically evaluate prefabricated versus 3D-printed composite resin veneers

详细描述

Dental veneers are now a commonly used conservative treatment to improve the appearance and functionality of anterior teeth that have enamel flaws, diastemas, small abnormalities, and discoloration. Compared to ceramic veneers, composite resin veneers have a number of benefits, such as requiring less tooth preparation, being less expensive, being easier to repair, and requiring less chairside time. Recent developments in composite resin technology and adhesive dentistry have further enhanced their mechanical qualities, wear resistance, and aesthetic results, making them a desirable treatment option for patients and professionals alike. There is little clinical data that directly compares the long-term performance of prefabricated and 3D-printed composite veneers, despite their growing use. The majority of research that is currently available has either examined each technique separately or has concentrated on laboratory assessments of mechanical properties. As a result, there is still not enough data to compare their clinical behavior in intraoral settings.

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 (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Good oral hygiene and satisfactory periodontal health
  • Patients requiring esthetic rehabilitation of anterior teeth
  • Presence of enough enamel for bonding

排除标准

  • Non-vital teeth or teeth requiring endodontic treatment
  • Severe malocclusion or parafunctional habits (e.g., bruxism or clenching)
  • Patients with severe intrinsic discoloration requiring alternative treatment

结局指标

主要结局

Color match and stability

时间窗: 24 months

Clinical evaluation of color match and color stability will be performed according to the World Dental Federation (FDI) evaluation criteria by two calibrated evaluators at baseline and at 6, 9, 12, and 24 months. Veneer restorations will be assigned FDI scores ranging from 1 (clinically excellent) to 5 (clinically poor). Clinical success will be considered as scores of 1-3 and failure as scores of 4-5. Assessment will be carried out under standardized lighting conditions using visual examination and magnification. Statistical analysis will be performed to compare changes over time and between the two study groups.

次要结局

未报告次要终点

研究者

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

Mohammed Abd El Ghany Mohammed

Principal Investigator

Tanta University

研究点 (1)

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