跳至主要内容
临床试验/NCT04370314
NCT04370314已完成不适用

Clinical Performance of One-piece Screw-retained Implant Crowns Base on CAD/CAM Hand-veneered Zirconium Dioxide Customized Abutments With a 6 Years and 7 Months Mean Follow-up

University of Bern1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2017年9月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
1
主要终点
Survival and success rates of all-ceramic implant-supported fixed reconstructions

研究概览

简要总结

Survival and success rates of all-ceramic implant-supported fixed reconstructions fabricated with CAD/CAM technology after at least one year in function.

Survival and success rates (clinical, radiologic and esthetic) of all-ceramic implant-supported fixed reconstructions fabricated with CAD/CAM technology after 2 to 10 years in function.

Establishment of a database of patients with all-ceramic implant-supported fixed reconstructions fabricated with CAD/CAM technology for future longitudinal retrospective studies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients with at least one fixed all-ceramic reconstruction (single implant restoration on BL implant with individualized zirconia abutment directly screwed and directly veneered, three- to five-unit zirconia bridges directly veneered, single tooth crown made of a lithium disilicate glass-ceramic (LS2) blank)
  • Written informed consent

排除标准

  • Pregnancy at the time of the follow-up examination
  • Mental handicap
  • Patients that could not be contacted/located
  • Patients not interested in participating
  • Patients with the need of antibiotic prophylaxis prior to a clinical examination

结局指标

主要结局

Survival and success rates of all-ceramic implant-supported fixed reconstructions

时间窗: 1 year

Number of all-ceramic implant-supported fixed reconstructions fabricated with CAD/CAM technology still in place after at least one year in function.

次要结局

  • Number of patients with biological complications assessed via clinical examination(1 year)
  • Number of patients with technical complications(1 year)
  • Number of patients with biological complications assessed via periapical x-ray(1 year)
  • Patient satisfaction as assessed by VAS A(1 year)
  • Patient satisfaction as assessed by VAS B(1 year)
  • Esthetic outcome(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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