Esthetics, Dental
Conditions
Interventions
This double-blind, randomized clinical trial compares the clinical performance of two flowable composite resins in non-carious cervical lesions (NCCL): the monochromatic flowable composite resin Vittr
42 individuals in the Opallis Flow group), with allocation made by software. Participants and evaluators will be blinded to the material used. Procedures include local anesthesia, absolute isolation,
E06.420.750
Sponsors
Universidade Estadual de Ponta Grossa
Universidade Estadual de Ponta Grossa
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Men and women; Good general health; 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 mm; and involve both the enamel and dentin of vital teeth; the cavosurface margin cannot involve more than 50% of the enamel; never having undergone dental whitening
Exclusion criteria
Exclusion criteria: Higiene oral extremamente pobre; usando dispositivos ortodônticos; periodontite severa ou crônica; hábitos de bruxismo pesado; alergia conhecida a materiais à base de resinas ou qualquer outro material usado neste estudo; mulheres grávidas ou lactantes; uso crônico de drogas anti-inflamatórias; analgésicas e psicotrópicas; paciente que já realizou clareamento dental
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 ContactMichael Favoreot
Universidade Estadual de Ponta Grossa
Outcome results
None listed