Tooth Diseases
Conditions
Interventions
Sixty participants with two non-carious cervical lesions side by side will undergo the interventions. There will be two groups (n=60). It is a randomized study. Randomization will be done intra-indivi
the cavities received Ambar Universal adhesive (FGM) according to the manufacturer's recommendations. Then, the c
E06.323.428
Sponsors
Universidade Estadual de Ponta Grossa
Universidade Estadual de Ponta Grossa
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Good general health;good oral hygiene;present at least 20 teeth under occlusion;at least two non-carious cervical lesions comparable in size;format and dimensions;non-retentive;deeper than half a mm;and involve both the enamel and dentin of vital teeth;The cavo-superficial margin cannot involve more than 50% of the enamel
Exclusion criteria
Exclusion criteria: Extremely poor oral hygiene;using orthodontic devices;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;analgesic 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
Public ContactAlessandro Loguercio
Universidade Estadual de Ponta Grossa
Outcome results
None listed