Two-unit Cantilever Implant Prostheses Made of Monolithic Zirconia or PFM

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorUniversity of Geneva, Switzerland

About this trial

The aim of is to compare the survival rate and technical outcomes of cantilever implant-supported fixed denture prosthetics (cFDPs) made either out of monolithic zirconia bonded to a titanium base in a digital workflow, or porcelain fused-to metal using a gold abutment in a conventional workflow. In addition, biological outcomes, wear patterns, PROMs and time efficiency will be recorded. The null hypothesis is: the reconstruction type does not influence the survival rate and technical outcomes of 2-unit implant-supported cFDP.

Eligibility criteria

Qualifiers

Minimal age of 22 years old.

No general medical condition which represents a contraindication to implant treatment

Good oral hygiene (PII ≤ 20%), and healthy periodontal tissues (BOP≤ 20%)

Two adjacent-teeth gap in posterior maxilla or mandible arch (first premolar, second premolar, first molar, second molar) with an osseointegrated regular or wide-diameter bone-level implant in a prosthetically correct position to allow occlusal screw-retention. Free-end edentulous gaps can also be included

Disqualifiers

Severe bruxism or clenching habits

Patients with inadequate oral hygiene or persistent intraoral infection

Women who are pregnant or breast feeding at the day of inclusion

Smokers exceeding 15 cigarettes / day, or equivalent; patients chewing tobacco

Trial design

Treatments tested in this trial

  • Monolithic zirconia screw retained implant-supported cantilever reconstruction supported by titanium base abutments, in a full digital workflow (ZR-TiB)
  • porcelain fused-to metal screw retained implant-supported cantilever reconstruction supported by a gold-abutment, in a conventional workflow (PFM-GA)

Treatment groups

38 Participants
are divided into 2 treatment groups

Sponsors and collaborators