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临床试验/NCT07330193
NCT07330193已完成不适用

Flowable Resin Composite: In Vitro Investigation of Antibacterial Effect and Calcium & Phosphorus Content and Two-Year Clinical Performance in Class I Restorations

Mansoura University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年6月22日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Modified FDI criteria

研究概览

简要总结

Evaluating Two-year clinical performance of class I restored with four different flowable resin composite restorations.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patients with bilateral occlusal small Class I carious lesions
  • • Good general health.
  • Patient aging 18-25 year.
  • Patient available for follow-up visits
  • Good oral hygiene

排除标准

  • Patients with orthodontic treatment
  • Severe or chronic periodontitis
  • Parafunctional habits
  • Sensitivity to resin-based material.
  • Poor oral hygiene.

研究组 & 干预措施

self adhesive flowable resin composite

Active Comparator

干预措施: Restoration with SARC (Procedure)

highly filled flowable resin composite

Active Comparator

干预措施: Restoration with HFFC (Procedure)

bioactive self adhesive flowable resin composite

Active Comparator

干预措施: Restoration with bioactive SARC (Procedure)

conventional flowable resin composite

Active Comparator

干预措施: Restoration with CFC (Procedure)

结局指标

主要结局

Modified FDI criteria

时间窗: two years

successful restorations percentage

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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