About this trial
The goal of this clinical trial is to to compare the prosthetic complication rate and Oral Health-Related Quality of Life (OHRQoL) between screw-retained monolithic zirconia frameworks and CNC-milled titanium frameworks with zirconia superstructures in completely edentulous patients restored with full-arch implant-supported prostheses over a follow-up period of 12 months.
Eligibility criteria
Qualifiers
Aged 18 years or older.
Able to understand the study procedures and provide written informed consent.
In good general health, classified as American Society of Anesthesiologists (ASA) Physical Status Class I or II.
Completely edentulous in the arch to be treated (maxilla and/or mandible).
Disqualifiers
Uncontrolled diabetes (HbA1c > 7.0%).
History of radiotherapy in the head and neck region.
History of intravenous bisphosphonate therapy.
Immunosuppressed or immunocompromised status.
Trial design
Treatments tested in this trial
- Monolithic Zirconia Prosthesis
- CNC-milled titanium framework and zirconia superstructure