Tooth Bleaching
Conditions
Interventions
This is a randomized, controlled, double-blind clinical trial with 42 participants with two non-carious cervical lesions side by side who were randomly distributed into two groups with allocation defi
the initial color of the teeth was assessed with a digital spectrophotometer before the intervention
dental whitening was performed in two office sessions with new measurements taken after each session and in subsequent follow-ups of 7, 14 and 30 days
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, 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; never having undergone dental whitening
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, analgesic and psychotropic drugs; patients who have already undergone dental whitening
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the color performance of a monochromatic composite resin versus a traditional composite resin using a digital spectrophotometer in non-carious cervical lesions before and after dental bleaching. Interim analyses of immediate data and at 6, 12, 24, 36 and 60 months will be performed | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the aesthetic properties; functional properties and biological properties using the World Dental Federation 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 Favoreto
Universidade Estadual de Ponta Grossa
Outcome results
None listed