Clinical evaluation of ceramic veneers manufactured by computed technology
- Conditions
- Tooth Discoloration, Dental caries, Dental Enamel Hypoplasia, Esthetics Dental.C07.650.800.255E06.420C07.793.735
- Registration Number
- RBR-8fgft5
- Lead Sponsor
- niversidade de São Paulo, Faculdade de Odontologia de Bauru
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients over 18 years;
Accordance with the TCLE;
Patients who have an indication for veneers: discoloration, tooth wear, fracture or anterior teeth with malformation;
Patients who have good general health during clinical evaluation period, good value mandibular and maxillary occlusal stability;
Patients who have need of treatment by at least two teeth and at most six teeth(region between canines).
History of allergy to any of the materials to be used in research
Drugs that could interfere with the oral environment;
Systemic or malignant diseases at the beginning of the study;
Inability to be subjected to specific techniques for performing the experiment not enough space for proper preparation of veneers;
Patients with parafunctional habits;
Patients with periodontitis severe gum inflammation;
Inadequate oral hygiene or high caries rates.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The veneers manufactured by compressed version and the CAD / CAM system do not show statistically significant differences in their clinical performance.<br>The veneers will be scored according to criteria of USPHS (United States Public Health Service): marginal adaptation, color change, marginal discoloration, restoration fracture, tooth fracture, wear restoration, antagonist wear, presence of caries and postoperative sensitivity.<br>The main variable is the marginal adaptation.
- Secondary Outcome Measures
Name Time Method Outcomes secondary are not expected