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临床试验/NCT05165563
NCT05165563已完成不适用

Comparison of Treatment Time Between Digital and Conventional Workflows for Treatment With Posterior Implant Restorations

Mahidol University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Treatment time

研究概览

简要总结

This randomized controlled trial (RCT) analyzed monolithic single-unit implant restorations out of lithium disilicate (LS2) or polymer-infiltrated ceramic networks (PICN) in a chairside digital workflow (Test) and a conventional protocol (Control). The primary outcome was to investigate the treatment time of the overall operation. The null hypothesis of this RCT was that both workflows had comparable results with respect to the defined outcomes.

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
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •The participants having a transmucosal implant system (Straumann TL RN/WN, Institut Straumann, AG, Basel, Switzerland) were placed in a single-tooth gap in the area of premolar or molar regions in the maxilla and mandible with existing interproximal and antagonist contacts.
  • •general medical health is healthy or has a well-controlled systemic disease.
  • •general oral health has shown no sign of infection or unsuccessfully treated diseases such as chronic periodontitis.

排除标准

  • •smoking more than 10 cigarettes per day.
  • •pregnancy.
  • •psychiatric disorder
  • •history of radiation therapy at the head and neck area.
  • •history of chemotherapy.
  • •history of bony pathologies such as osseous dysplasia, odontogenic cyst or tumor, etc.

研究组 & 干预措施

Workflows

Experimental

Digital and conventional workflows for treatment of implant single crowns

干预措施: Treatment of implant single crown (Procedure)

Materials

Experimental

Materials for treatment of implant single crowns (polymer-infiltrated ceramic networks, PICNs and lithium disilicate, LS2).

干预措施: Treatment of implant single crown (Procedure)

结局指标

主要结局

Treatment time

时间窗: First visit to prosthesis delivery visit, through study completion, an average of 1 month

Treatment time in every steps were recorded.

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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