The aim of the study is to prospectively evaluate the survival of JJGC Cobalt-Chromium (CoCr) prosthetic abutments in single-unit implant-supported prostheses, to confirm the long-term safety and performance of the devices.
The cobalt-chromium prosthetic abutments are designed to be installed between the implant and prosthesis. CoCr abutment coping, CoCr abutment for crown set, block and CARES® are devices with indication for prostheses. Data from the scientific literature support the safety and intended performance of these abutments. An observational clinical study design was chosen to augment the clinical data derived from the use of these devices in accordance with the IFU (Instruction for Use) in the daily clinical practice setting, as well as to assess the long-term prosthetic survival rate.
Study Type
OBSERVATIONAL
Enrollment
167
Cobalt-Chromium (CoCr) prosthetic abutments in single-unit implant-supported prostheses
Instituto Latino Americano de Pesquisa e Ensino Odontológico (ILAPEO)
Curitiba, Brazil
RECRUITINGProsthesis survival arte
Evaluation of the survival rate of implant-supported prostheses using CoCr prosthetic abutments.
Time frame: 24 months after provisional prosthesis installation
Implant survival rate
Survival rate of implant rehabilitated with prosthesis using CoCr abutments
Time frame: 24 months after provisional prosthesis installation
Implant success rate
Success rate of implant rehabilitated with prosthesis using CoCr abutments
Time frame: 24 months after provisional prosthesis installation
Patient satisfaction
Patient satisfaction with the treatment
Time frame: 24 months after provisional prosthesis installation
Clinician Satisfaction
Surgeon satisfaction after the installation of the prosthesis regarding the devices used
Time frame: 24 months after provisional prosthesis installation
Adverse events
• Occurrence of adverse events, device deficiencies and residual risks related to abutments, prostheses, and oral health.
Time frame: 24 months after provisional prosthesis installation
Risk factors
Influence of risk factors on observed results
Time frame: 24 months after provisional prosthesis installation
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