Dentin Sensitivity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients of both sexes were included in the present study; aged between 18 and 40 years; who had at least six upper anterior teeth free of caries and restorations on the buccal surface; central or canine incisor with A2 or darker coloration; satisfactory oral hygiene; absence of periodontal disease.
Exclusion criteria
Exclusion criteria: The individuals excluded from the study were users of fixed orthodontic appliances; pregnant women; lactating women; severe intrinsic stains on teeth (stains due to tetracycline, fluorosis and pulped teeth); who were consuming any anti-inflammatory and antioxidant drugs; using desensitizing toothpaste; participants with a previous history of tooth sensitivity or any associated pathology (bruxism, gingival recession, noncarious lesion with dentin exposure).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of patients that report spontaneous pain in any moment of the bleaching protocol and up to 48 h post-bleaching, through self-report. This number will be presented as percentage of patients with tooth sensitivity and will be named absolute risk of tooth sensitivity.;The intensity of tooth sensitivity will be assessed using the visual analogue scale (VAS 0-10) and will be presented as means and standard deviations in different periods (during dental bleaching, up to 1 h, 1 h to 24 h and 24 h to 48 h post-bleaching). | — |
Secondary
| Measure | Time frame |
|---|---|
| The difference in color between the baseline condition and post-bleaching (1 week and 1 month) will be assessed by Vita Classical and Bleachedguide Vita shade guide as well as with the Vita Easyshade spectrophotometer. The data will be presented as means and standard deviations. | — |
Countries
Brazil
Contacts
Universidade Federal do Amazonas