Dental Implant Failed, Dental Prosthesis Failure
Conditions
Keywords
CAD-CAM, composite dental resin, Immediate dental implant loading
Brief summary
This study evaluates the success rate, as the biological and prosthesis complications, of posterior single-unit implants immediately loaded with a chair side Computer-Aided Design and Manufacturing (CAD-CAM) composite crown, after a follow-up period of 6 months,1,2,3,4 and 5 years. Complementary ex vivo analyses will be performed to evaluate the wear of restorations. The time and cost benefit of the presented digital workflow, as patient centered outcomes will also be evaluated.
Interventions
DEVICEimmediate loading of posterior implants with chairside CAD-CAM composite crown
Sponsors
University of Liege
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
0 In good systemic health (ASA I/ II) * Present with no contra indication against oral surgical interventions * The tooth at the implant site(s) must have been extracted or lost at least 12 weeks before the date of implantation. * At least 8 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%
Exclusion criteria
* Autoimmune disease requiring medical treatment * Medical conditions requiring prolonged use of steroids * Use of Bisphosphonate intravenously or more then ˃ 3 years of oral use * 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 * Smokers * Prisoners * Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance, or unreliability. Local
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Implant complication rate | 6 months |
| Prosthesis complication rate | 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of treatment duration, timing (in minutes) all the different steps of the surgical and prosthodontic procedure. | 1 day |
| Evaluation of patient satisfaction with VAS (visual analog scale) questionnaire | 1 day |
Countries
Belgium
Contacts
Primary ContactAmélie Mainjot
Backup ContactFrance Lambert
Outcome results
None listed