Dentin Sensivity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy volunteers; both genders; minimum age of 18 years and maximum without limit; non smokers; have vital teeth free of carious lesions; non-carious in the anterior region; free from periodontal disease; and the upper right canine should be A2 or darker in color compared to the Vita Classical scale; patients must sign the Informed Consent Form after explaining the details of the research
Exclusion criteria
Exclusion criteria: Volunteers with previous tooth sensitivity; who never performed any type of dental bleaching; smokers, pregnant or breastfeeding women; in continuous use of medications such as analgesics or anti-inflammatories; who do not use prostheses; no restorations on the upper anterior teeth; are not using fixed orthodontic appliance; without any parafunction; no gingival recession; no endodontic treatment of anterior teeth, no severe dental discoloration (tetracycline staining or fluorosis) and visible cracks in teeth
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The will initially assess the absolute risk of tooth sensitivity resulting from professional tooth bleaching when associated with homemade. According to a systematic review of clinical studies that evaluated tooth sensitivity when associated with inpatient tooth bleaching when associated with a trained caretaker, 88% of patients had tooth sensitivity at least once during the whitening procedure. To detect a reduction in the primary outcome from 88% in the control group to 68% in the experimental group, a minimum total of 64 volunteers will be required, with a power of 80% and an alpha of 5%. To contemplate possible follow-up losses, another 16 volunteers per group (25%) will be added, totaling 80 volunteers per group | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Countries
Brazil
Contacts
Universidade Ceuma