Single Tooth Lost
Conditions
Brief summary
Objectives - To evaluate the 4-year clinical outcomes of ceramic veneered Computer Aided Design/Computer Aided Manufacturing (CAD/CAM) Co-Cr single crowns supported by natural teeth in posterior regions. Material and methods - Eighty-nine patients were provided with 120 ceramic veneered CAD/CAM Co-Cr single crowns replacing either premolars and molars. Specific inclusion criteria were needed and tooth preparations were standardized and performed by 2 expert prosthodontists. CAD/CAM Co-Cr frameworks were fabricated and veneered with ceramics. The restorations were cemented using a eugenol-free zinc oxide luting agent. The patients were recalled after 1, 6, 12, 24, 36 and 48 months. The survival and success of the restorations were evaluated. The technical and esthetic outcomes were examined using the United States Public Health Service criteria. The biologic outcomes were analyzed at abutment and contralateral teeth and descriptive statistics were performed.
Interventions
DEVICECo-Cr single crown
OTHERPeriodontal parameters
Sponsors
Federico II University
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
21 Years to 68 Years
Healthy volunteers
No
Inclusion criteria
* good general health * American Society of Anesthesiologists (ASA) ASA I or ASA II condition; periodontal health * Angle class I occlusal relationship * minimum of 10 couples of opponent teeth * good oral hygiene * no evident signs of parafunctions and/or temporomandibular disorders. * periodontal health of abutment teeth (absence of tooth mobility, absence of furcation involvement); * proper positioning of abutment teeth in the dental arch (tooth axis adequate for a SC) * sufficient occlusal-cervical height of the clinical crown of abutment teeth (≥ 4 mm) for the retention of a SC * vital or endodontically treated to a clinically sound state abutment teeth; * abutment teeth opposing natural teeth.
Exclusion criteria
* high caries activity * presence of periodontal disease on the abutment tooth * occlusal-cervical height of the abutment tooth \< 4 mm * reduced interocclusal distance or supraerupted opposing teeth * unfavorable crown-to-root ratio * severe were facets, clenching and/or bruxism * presence of removable partial dentures (RPDs) * pregnancy or lactation * alcohol and/or drug addiction
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival percentage | 4 years | Kaplan Meier analysis of survival of the prostheses |
Outcome results
None listed