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临床试验/NCT07691905
NCT07691905进行中(未招募)不适用

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

Hue University of Medicine and Pharmacy1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年1月4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
120
试验地点
1
主要终点
Gingival index

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
3 Years 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

Gingival index

时间窗: 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.

Fluorescent Plaque Index

时间窗: 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.

Opposing Tooth Wear

时间窗: 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.

Crown Retention

时间窗: 3, 6, and 12 months after crown placement

Retention status of the prefabricated crown, categorized as retained or loose/lost.

Clinical Status of Crowned Teeth

时间窗: 3, 6, and 12 months after crown placement

Clinical status of teeth restored with prefabricated crowns, categorized as asymptomatic, sensitive, mobile, painful, or swollen.

次要结局

  • Parental Satisfaction(6 and 12 months after crown placement)

研究者

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

Le Van Nhat Thang

Principal Investigator

Hue University of Medicine and Pharmacy

研究点 (1)

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