Composite Resins
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Minimum age of 18 years; both genders; good oral hygiene; present at least 20 teeth under occlusion; at least two non-carious cervical lesions comparable in size, shape and dimensions; non-retentive; deeper than half a millimeter; involve both the enamel and dentin of vital teeth; the cavosurface margin cannot involve more than 50% of the enamel
Exclusion criteria
Exclusion criteria: Extremely poor oral hygiene; wearing orthodontic appliances; severe or chronic periodontitis; heavy bruxism habits; known allergy to resin-based materials or any other material used in this study; pregnant or lactating women; chronic use of anti-inflammatory drugs; analgesics and psychotropic drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate color match using a digital spectrophotometer on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed immediate and 6, 12, 24, 36 and 60 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the aesthetic properties; functional properties and biological properties using the World Dental Federation (FDI) clinical criteria on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed immediate and 6, 12, 24, 36 and 60 months. | — |
Countries
Brazil
Contacts
Universidade Estadual de Ponta Grossa