跳至主要内容
临床试验/NCT03234868
NCT03234868已完成4 期

Benefit of the Digital Workflow for Screw-retained Single Implant Restorations

University of Liege0 个研究点目标入组 34 人开始时间: 2016年1月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
34
主要终点
Fit of the crowns

研究概览

简要总结

The aim of this research project is emphasize the benefit of the digital workflow compared to conventional impressions and crown processing with standard la procedures. The objectives of the present study are to measure and compare the global cost, the time spent in the dental chair and in the lab and the fit of both digital and conventional workflow. Additionally, patient centered outcomes will be recorded.

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
None

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •Subject must have voluntarily signed the informed consent form before any study related action
  • •Age: 18 with one or more missing teeth in the maxillary area, seeking for implant therapy.
  • •Men/Women
  • •In good systemic health (ASA I/ II)
  • •Present with no contra indication against oral surgical interventions
  • •Patients required replacement of a single missing tooth. The tooth at the implant site(s) must have been extracted or lost at least 12 weeks before the date of implantation.
  • •At least 10 mm of bone in the vertical dimension
  • •At least 6 mm of bone in the bucco-lingual dimension.
  • •No need for bone augmentation procedure in any of the dimensions
  • •Full mouth plaque score (FMPI) lower or equal than 25%

排除标准

  • •Autoimmune disease require medical treatment
  • •Medical conditions requiring prolonged use of steroids
  • •Use of Bisphosphonate intravenously or more then
  • •Infection (local or systemic) - patient with gingivitis or active local infection will undergo a medical treatment prior to his entrance to the study, each individual will be evaluated prior to study procedure for suitability, in case of systemic infection the evaluation will be based on medical anamneses, and if necessary will be referred to relevant medical tests.
  • •Current pregnancy or breastfeeding women
  • •Alcoholism or chronically drug abuse
  • •Immunocompromised patients
  • •Uncontrolled Diabetes
  • •Prisoners

研究组 & 干预措施

Optical impression

Experimental

The optical impression system used for the study is TRIOS (3 shape). First of all, the operators in charge of taking the digital impressions are going to get trained prior the study and will calibrate (learning curve). MIS Scan bodies will be placed on the multi-unit plaforms, an x-ray will be taken in order to check the fit) and the impression will be realised following the instruction given by the system (first the maxillary and mandibular impressions followed by the bite registration). Shade will be chosen using VITA toothguide 3D master (to pick the right zirconia shade).

干预措施: Impression procedure (Device)

Conventional impression

Active Comparator

Once the impression coping is placed on the multi-unit plaform, the fit will be checked with an intra-oral X-ray. The impressions will be made with medium viscosity silicon. As a second step, alginate antagonist impression will be done. Bite will not be recorded (single tooth missing). The two impressions will be placed in a hermetic plastic bag and send to lab. Shade will be chosen using VITA toothguide 3D master.

干预措施: Impression procedure (Device)

Digital workflow

Experimental

The implant crowns issued from digital impressions will be done according a cast less / full digital workflow. The STL files collected from the TRIOS will be sent directly to the lab. The designing of the full zirconia crowns will be performed in the TRIOS 3SHAPE program. The resulting files will be sent to the CAM unit production (Amman Girrbach milling machine & MAZAK CNC machine: Mcenter to be specify (Berlin or Israel) to be milled (milled & sintered only) considering the direct adaption for a Multi-Unit connection. A superficial make-up will be done on the monolithic crown in the lab. And finally, the products will be delivered to the dentist.

干预措施: Crown manufacturing procedures (Device)

Conventional workflow

Active Comparator

The implant crowns issued from conventional impressions will be realised by sending the impressions to the lab (Mirko Picone). The lab will pour the impressions in dental stone (class 4 scannable without powdering: extra hard and scanning powder included). Then, the technician will realize a mock-up of the crown's framework on a temporary abutment in DuraLay Resin.

The mock up will be scanned with ZIRKONZAHN scanner (or equivalent) and send this information to a central fabrication facility for milling (Amman Girrbach milling machine & MAZAK CNC machine:

Mcenter: to be specify (Berlin or Israel). The lab technician will get the Zi framework back and will apply veneer ceramic.

干预措施: Crown manufacturing procedures (Device)

结局指标

主要结局

Fit of the crowns

时间窗: 1 year

To measure this parameter we will focus on interproximal fit and occlusion. Interproximal contact points will be checked with dental floss.

次要结局

  • Global cost(1 year)
  • Esthetical aspect(1 year)
  • Patient centered outcomes(1 year)
  • Time consumption at the dental chair(1 year)
  • Time consumption in the lab(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. France LAMBERT

Prof.

University of Liege

相似试验