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Clinical Trial Summary

The aim of the present study is to test whether or not the use of translucent monolithic zirconia crowns bonded to a titanium base abutment perform similar to porcelain-fused-to-metal crowns on single implants in the posterior region.


Clinical Trial Description

In the majority of studies on implant-supported restorations, a considerable rate of fractures of the veneering ceramic was reported. The clinical data is restricted to full-ceramic implant-supported reconstructions in the anterior region. No clinical data is available on the performance of full-ceramic restorations in the molar region. The use of translucent monolithic zirconia for implant-supported crowns (without veneering ceramic) may reduce the technical complication rate and allow for sufficient aesthetic results in the molar region. To date, no clinical trial investigating monolithic zirconia crowns for single molar implants is available. The primary outcome of the study is the technical complication rate. This outcome represents an indicator for the prosthetic success of the implant-supported crown. The main biological secondary outcomes are marginal bone level, histological signs of inflammation, and presence of pathogenic bacteria. Further outcomes are crown survival, wear of the crown and of the antagonist. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02272491
Study type Interventional
Source University of Zurich
Contact
Status Active, not recruiting
Phase N/A
Start date October 2014
Completion date November 1, 2027

See also
  Status Clinical Trial Phase
Completed NCT01644630 - To Compare Cemented Versus Screw-retained Implant-supported Single Crowns With Customized Zirconia Abutments N/A