Pathological conditions, signs and symptoms
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy volunteers; non smokers; both genders; intact permanent teeth without cavities or restorations; teeth with pulp vitality without internal resorption or calcification; teeth with complete root apex without signs of periodontal or periapical lesions
Exclusion criteria
Exclusion criteria: Smoking patients; patients who suffered external tooth whitening; patients with parafunctional habits; patients with a history of dental trauma; pregnant women; lactating women; patients using orthodontic appliances; patients with previous dental pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find changes in the pulp oxygen saturation levels, observed with the use of the pulse oximeter, from the observation of a variation of at least 5% in the pre and post-intervention measurements (use of the bleaching gels). | — |
Secondary
| Measure | Time frame |
|---|---|
| Check the increase in the painful sensitivity of the dental elements, with the use of an analogue pain scale completed by the patient after each intervention, based on the observation of a variation of at least 5% in the pre and post-intervention measurements.;It is expected to verify less dental sensitivity with the use of the whitening gel associated with the desensitizer, by comparing the results obtained between the whitening gels, after the filling of the analogue pain scale by the patients, from the finding of a variation of at least 5% in the patients. pre- and post-intervention results. | — |
Countries
Brazil
Contacts
Universidade Federal de Santa Catarina