A clinical study to assess the durability dental restorations made with bioactive restorative materials: a randomized clinical trial
Phase 4
Recruiting
- Conditions
- dental cariesC07.793.720.210
- Registration Number
- RBR-2hqhdp
- Lead Sponsor
- Instituto de Ciência e Tecnologia - Universidade Estadual Paulista
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients 12 to 50 years old able to provide valid information; who require at least one class II dental restoration due to active carious lesion or exchange for poor permanent tooth restoration; the tooth selected to receive the restoration must have an antagonist and adjacent tooth; without excessive tooth wear; without evident temporomandibular disorders.
Exclusion Criteria
Start orthodontics during the course of the research; present allergy to any material used in the research.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Retention failure of composite restorations will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months;The presence of the fracture of the restoration will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months
- Secondary Outcome Measures
Name Time Method The presence of the Marginal discoloration of the restoration will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months<br>;The presence of the recurrence caries will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months