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临床试验/NCT07524842
NCT07524842尚未招募不适用

Clinical Performance of Three Different Restorative Materials-Nanohybrid, Bulk-fill, and Alkasite-based

Hacettepe University0 个研究点目标入组 60 人开始时间: 2026年4月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Clinical performances of different restorative systems according to FDI criteria

研究概览

简要总结

The clinical performance of a bioactive composite (alkasite-based), a nanohybrid resin composite and a bulk-fill resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 3 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into three groups: a bioactive composite [Cention Forte Ivoclar Vivadent, Schaan, Liechtenstein], a nanohybrid resin composite [Tetric N-Ceram2 (Ivoclar Vivadent, Schaan, Liechtenstein)] and a bulk-fill resin composite [Tetric N-PowerFill2 (Ivoclar Vivadent, Schaan, Liechtenstein)], All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

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 (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age range will be 18 to 65
  • patients should have at least 3 approximal caries lesions require restoration
  • healthy periodontal status
  • a good likelihood of recall availability

排除标准

  • poor gingival health
  • adverse medical history
  • potential behavioral problems

研究组 & 干预措施

bioactive composite

Experimental

Cention Forte Ivoclar Vivadent, Schaan, Liechtenstein

干预措施: bioactive composite (Device)

nanohybrid resin composite

Experimental

Tetric N-Ceram2 (Ivoclar Vivadent, Schaan, Liechtenstein)

干预措施: nanohybrid resin composite (Device)

bulk-fill resin composite

Experimental

Tetric N-PowerFill2 (Ivoclar Vivadent, Schaan, Liechtenstein)

干预措施: bulk-fill resin composite (Device)

结局指标

主要结局

Clinical performances of different restorative systems according to FDI criteria

时间窗: two years

Two year results according to FDI criteria (scores 1-5, 1-very good, 5-poor/replace)

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

Dr. Fatma Dilşad Öz

Prof. Dr.

Hacettepe University

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