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Zirconia and Bioflx Crowns for Primary Anterior Teeth

2026年7月2日 更新者:Le Van Nhat Thang、Hue University of Medicine and Pharmacy

Clinical Outcomes of Prefabricated Zirconia and Bioflx Crowns for Restoring Primary Maxillary Anterior Teeth: A Randomized Controlled Trial

This parallel-group randomized controlled trial will compare the clinical performance of prefabricated zirconia and Bioflx crowns for restoring primary maxillary anterior teeth in children aged 3 to 5 years. Eligible participants will be randomly assigned in a 1:1 ratio to receive either a zirconia crown or a Bioflx crown.

Clinical outcomes will be assessed at 3, 6, and 12 months after crown placement. Evaluations will include gingival health, plaque accumulation, wear of the opposing tooth, crown retention, and clinical symptoms of the treated tooth. Parent satisfaction with the esthetic outcome will also be evaluated.

The study aims to provide comparative clinical evidence on the effectiveness of zirconia and Bioflx crowns for restoration of primary maxillary anterior teeth.

研究概览

详细说明

Primary maxillary anterior teeth are important for esthetics, speech, mastication, and maintenance of normal oral function in young children. Extensive caries and hypomineralization may result in substantial loss of tooth structure and require full-coverage restoration. Prefabricated zirconia and Bioflx crowns are esthetic restorative options; however, comparative clinical evidence for their use in primary maxillary anterior teeth remains limited.

This study is a parallel-group randomized controlled clinical trial conducted in children aged 3 to 5 years who require full-coverage restoration of primary maxillary anterior teeth. Eligible participants must have an opposing tooth and at least two carious surfaces on the target tooth, caries involving the incisal edge, or discoloration associated with hypomineralization. Children with acute systemic disease, allergy to the luting cement, pulp exposure before treatment, inadequate remaining tooth structure, severe bruxism or deep bite, advanced root resorption, previous trauma affecting the target tooth, or other predefined exclusion criteria will not be enrolled.

A minimum of 120 teeth will be included. Randomization will be performed at the participant level using a computer-generated variable block sequence with a 1:1 allocation ratio. Allocation concealment will be maintained using sequentially numbered opaque sealed envelopes.

Participants will receive either prefabricated zirconia crowns or prefabricated Bioflx crowns. Clinical and radiographic examinations will be completed before treatment. Crown preparation and cementation procedures will be standardized, and Fuji IX Extra glass ionomer cement will be used for crown placement.

The primary outcome will be gingival health at 6 months after crown placement. Secondary outcomes will include plaque accumulation, wear of opposing teeth, crown retention, clinical symptoms of crowned teeth, and parent satisfaction with crown esthetics. Follow-up assessments will be performed at 3, 6, and 12 months. Statistical analyses will account for clustering when more than one tooth is included from the same participant.

研究类型

介入性

注册 (估计的)

120

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Huế、越南、530000
        • Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

不

描述

Inclusion Criteria:

  • Children aged 3 to 5 years.
  • Children requiring full-coverage restoration of one or more primary maxillary anterior teeth.
  • Presence of an opposing tooth.
  • Target tooth with at least two carious surfaces, caries involving the incisal edge, or discoloration associated with hypomineralization.
  • Written informed consent from a parent or legal guardian and willingness to comply with treatment and follow-up visits.

Exclusion Criteria:

  • Allergy to Fuji IX Extra glass ionomer cement.
  • Acute systemic disease.
  • Crowded teeth affecting crown placement.
  • Pulp exposure before treatment.
  • Inadequate remaining clinical crown structure after tooth preparation.
  • Absence of an opposing tooth.
  • Bruxism or deep bite.
  • Tooth close to exfoliation or root resorption exceeding one-half of the root length.
  • Caries limited to a single surface without proximal involvement.
  • History of trauma affecting the target tooth.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Zirconia
Participants receive prefabricated zirconia crowns for restoration of indicated primary maxillary anterior teeth. Teeth are prepared using a standardized clinical protocol, and crowns are cemented with Fuji IX Extra glass ionomer cement.
Prefabricated zirconia crowns manufactured by Shinhung, Republic of Korea, will be used to restore eligible primary maxillary anterior teeth. Tooth preparation, crown selection, cementation with Fuji IX Extra glass ionomer cement, removal of excess cement, and post-treatment instructions will follow a standardized protocol.
实验性的:Bioflx
Participants receive prefabricated Bioflx crowns for restoration of indicated primary maxillary anterior teeth. Teeth are prepared using a standardized clinical protocol, and crowns are cemented with Fuji IX Extra glass ionomer cement.
Prefabricated Bioflx crowns manufactured by Kids-e-Dental, India, will be used to restore eligible primary maxillary anterior teeth. Tooth preparation, crown selection, cementation with Fuji IX Extra glass ionomer cement, removal of excess cement, and post-treatment instructions will follow a standardized protocol.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Gingival index
大体时间:3, 6, and 12 months after crown placement
Gingival status adjacent to crowned primary maxillary anterior teeth, assessed using the Löe and Silness Gingival Index. Lower scores indicate better gingival health.
3, 6, and 12 months after crown placement
Fluorescent Plaque Index
大体时间:3, 6, and 12 months after crown placement
Plaque accumulation on crowned primary maxillary anterior teeth, assessed using QrayScan Plus according to the Fluorescent Plaque Index (FPI; 0-5). Higher scores indicate greater plaque accumulation.
3, 6, and 12 months after crown placement
Opposing Tooth Wear
大体时间:3, 6, and 12 months after crown placement
Wear of the tooth opposing the crowned primary maxillary anterior tooth, assessed clinically on a 0-4 ordinal scale. Higher scores indicate greater enamel and dentin loss.
3, 6, and 12 months after crown placement
Crown Retention
大体时间:3, 6, and 12 months after crown placement
Retention status of the prefabricated crown, categorized as retained or loose/lost.
3, 6, and 12 months after crown placement
Clinical Status of Crowned Teeth
大体时间:3, 6, and 12 months after crown placement
Clinical status of teeth restored with prefabricated crowns, categorized as asymptomatic, sensitive, mobile, painful, or swollen.
3, 6, and 12 months after crown placement

次要结果测量

结果测量
措施说明
大体时间
Parental Satisfaction
大体时间:6 and 12 months after crown placement
Parental satisfaction with the esthetic outcome of crown restoration, assessed using a 4-point Likert scale for crown shape, color, alignment, interdental spacing, perceived crowding, and other esthetic abnormalities. Lower scores indicate greater satisfaction.
6 and 12 months after crown placement

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年1月4日

初级完成 (估计的)

2027年4月1日

研究完成 (估计的)

2027年4月1日

研究注册日期

首次提交

2026年7月2日

首先提交符合 QC 标准的

2026年7月2日

首次发布 (实际的)

2026年7月9日

研究记录更新

最后更新发布 (实际的)

2026年7月9日

上次提交的符合 QC 标准的更新

2026年7月2日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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