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临床试验/NCT04298151
NCT04298151已完成2 期

Clinical Evaluation of Zirconia Reinforced Versus Conventional Viscous Glass Ionomer in Posterior Restorations of Geriatric Patients: 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: 2021年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
28
试验地点
1
主要终点
Clinical performance

研究概览

简要总结

This study is conducted to evaluate the clinical performance of Zirconomer Improved GI restoration compared to Conventional viscous GI restoration in geriatric patients with Posterior carious lesions in class I or II cavities

详细描述

This study will be conducted to determine the clinical performance of the Zirconia reinforced glass ionomer restorations ( Zirconomer improved) under stress bearing posterior area (class I or claa II cavities) in geriatric population in comparison to Conventional viscous glass ionomer restorations (Ketac molar quick Aplicap) using the modified United States Public Health Service (USPHS) criteria

P: Geriatric Patients with posterior Caries lesions I: Zirconia reinforced GI (Zirconomer Improved) C: Conventional viscous GI, (Ketac Molar quick Aplicap) O: The Clinical performance of the Glass Ionomer restorations Using USPHS Criteria

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)

入排标准

年龄范围
60 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age range 60-80 years
  • Geriatric patients with Class I or II Posterior carious lesions.
  • Males or Females.
  • Pulp asymptomatic vital carious posterior teeth.
  • Co-operative patients approving to participate in the trial.

排除标准

  • Age range less than 60 years.
  • Disabilities.
  • Deep extensive carious cavities that may lead to fracture of the tooth or pulpal affection.
  • Teeth with signs and symptoms of irreversible pulpitis or pulp necrosis.
  • Heavy smoking.
  • Lack of compliance.

研究组 & 干预措施

zirconomer improved

Experimental

zirconia reinforced glass ionomer restoration

干预措施: Zirconomer Improved (Drug)

ketac molar quick aplicap

Active Comparator

conventional viscous glass ionomer restoration

干预措施: Ketac Molar quick Aplicap (Drug)

结局指标

主要结局

Clinical performance

时间窗: 1 year

clinical performance of the Glass Ionomer restorations using modified USPHS criteria

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

Doaa Mohammed Mohammed Abdou

Assistant lecturer

Cairo University

研究点 (1)

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