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临床试验/NCT07436325
NCT07436325Enrolling By Invitation不适用

Comparison of Gingival Health Outcomes Between Prefabricated Zirconia Crowns and Stainless Steel Crowns in Primary Molars: A Randomized Split-Mouth Clinical Trial

Murad Alrashidi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年5月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
100
试验地点
1
主要终点
Change in Gingival Health

研究概览

简要总结

The goal of this clinical trial is to learn if prefabricated zirconia crowns (PZCs) improve gingival health compared to stainless steel crowns (SSCs) in primary molars of young children. It will also learn about plaque accumulation and parental satisfaction with the crowns. The main questions it aims to answer are:

  1. Do PZCs lead to better gingival health than SSCs over time?
  2. Do PZCs reduce plaque accumulation compared to SSCs?
  3. Do parents report higher satisfaction with PZCs versus SSCs?

Researchers will compare PZCs to SSCs in a split-mouth design (each child receives one of each crown type on contralateral molars) to see if PZCs provide superior gingival health, plaque control, and satisfaction.

Participants will:

  1. Receive PZCs on one primary molar and SSCs on the contralateral molar after tooth preparation
  2. Attend follow-up visits at 12, 24, and 36 months for gingival health and plaque assessments
  3. Complete parental satisfaction surveys at each follow-up visit

详细描述

This clinical trial is a prospective, randomized, split-mouth controlled study designed to compare the long-term effects of prefabricated zirconia crowns (PZCs) and stainless steel crowns (SSCs) on gingival health, plaque accumulation, and parental satisfaction in primary molars of young children. The study addresses the need for evidence on how these restorative materials influence periodontal outcomes, given the conflicting data in existing literature regarding their biocompatibility, esthetics, and impact on gingival tissues. SSCs have been the standard for durability and cost-effectiveness in pediatric dentistry, but their metallic appearance and potential for plaque retention due to marginal microgaps raise concerns for esthetics and gingival inflammation. PZCs, offering superior esthetics and a polished surface, may provide advantages in reducing plaque adherence and improving mucosal compatibility, though long-term comparative data are limited.

This trial will employ a split-mouth design at the Pediatric Dental Clinic of Qassim University, Buraydah, Al-Qassim Province, Saudi Arabia. This intra-subject approach minimizes inter-individual variability in factors such as salivary composition, microbial ecology, brushing habits, dietary sugar intake, and systemic health, enabling direct comparison of the two crown types within the same child. One hundred healthy children with bilateral primary molars requiring full-coverage restorations will be enrolled. Randomization using a computer-generated sequence with allocation concealment via opaque envelopes opened chairside post-preparation will be implemented. Contralateral molars will receive either a PZC or SSC (randomly assigned), ensuring balanced distribution.

Tooth preparation will be standardized under local anesthesia (2% lidocaine with 1:100,000 epinephrine): pulpotomy/pulpectomy as indicated, circumferential reduction (1-1.5 mm) with tapered diamond burs, occlusal clearance (1.5-2 mm), and proximal adjustments. PZCs will be fitted without crimping for optimal marginal adaptation (<50 μm target), while SSCs will undergo mechanical crimping for tight cervical fit (<30 μm discrepancy). Both will be luted with resin-modified glass ionomer cement (RelyX™ Luting Plus, 3M™) for fluoride release and reliable bonding. Assessments will be conducted by two independent, calibrated examiners (inter-rater kappa >0.80) blinded to crown type via opaque cheek retractors.

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)

入排标准

年龄范围
3 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy children aged 3-7 years.
  • Bilateral primary molars requiring full-coverage restorations.
  • Adequate tooth structure (>50% remaining post-preparation).

排除标准

  • Children with moderate to severe baseline plaque accumulation (Silness & Löe Plaque Index ≥2) or parents/caregivers reporting inconsistent brushing (<2x/day).
  • Children with excessive sugar intake (>3 sugary snacks/beverages daily), assessed via the Beverage and Snack Questionnaire.
  • Systemic diseases affecting oral health (e.g., immunocompromised status, diabetes mellitus).
  • Active periodontal disease or severe malocclusion.
  • Allergy to crown materials.

研究组 & 干预措施

Experimental arm (Prefabricated zirconia crowns)

Experimental

The experimental arm in this split-mouth randomized clinical trial involves the placement of prefabricated zirconia crowns (PZCs; specifically NuSmile® ZR) on one primary molar per participant.

干预措施: Prefabricated Zirconia Crown (Procedure)

Active comparator arm (Stainless steel crowns)

Active Comparator

The comparator arm (active control) in this split-mouth randomized clinical trial involves the placement of stainless steel crowns (SSCs; specifically 3M™ ESPE™) on the contralateral primary molar per participant

干预措施: Stainless steel crown (Procedure)

结局指标

主要结局

Change in Gingival Health

时间窗: Baseline, 12 months, 24 months, and 36 months

Gingival health assessed using the Löe Gingival Index. Four sites per tooth (mesial, distal, buccal, lingual) are scored as follows: 0 = Normal gingiva (no inflammation) 1. = Mild inflammation - slight change in color, slight edema, no bleeding on probing 2. = Moderate inflammation - redness, edema, glazing, bleeding on probing 3. = Severe inflammation - marked redness and edema, ulceration, tendency to spontaneous bleeding Mean score per tooth (or per participant across assessed sites) is calculated. Higher scores indicate worse gingival inflammation. This primary outcome evaluates the comparative effect of prefabricated zirconia crowns versus stainless steel crowns on gingival tissue response over time, with assessments performed by blinded calibrated examiners.

次要结局

  • Plaque Index Score(Baseline, 12 months, 24 months, and 36 months)

研究者

发起方
Murad Alrashidi
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Murad Alrashidi

Assistant Professor, Department of Orthodontic and Peadiatric dentistry, College of Dentistry, Qassim University, Saudi Arabia

Qassim University

研究点 (1)

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