Dentin Sensitivity
Conditions
Interventions
The distribution process will be carried out using Microsoft Excel software, in which the average of initial scores of dental sensitivity obtained through the VAS for all selected teeth will be calcul
Sponsors
Faculdade de Odontologia de Bauru - Universidade de São Paulo
Faculdade de Odontologia de Bauru - Universidade de São Paulo
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Participants who have at least one tooth with dentin hypersensitivity, with a score equal to or greater than 4 on the Analogic Visual Scale (VAS). Participants must be aged between 18 and 65. Both genders. Having overall good health. Being available to attend the scheduled appointments and treatment sessions throughout the study period
Exclusion criteria
Exclusion criteria: Individuals with active caries lesions and/or defective restorations on the selected and/or adjacent teeth; structural dentin loss requiring restoration or periodontal treatment; prior use of professional desensitizing agents in the last 6 months; smokers; pregnant individuals; those using anti-inflammatory and/or analgesic medications during the study period - or up to 72 hours before the initial assessment; those who regularly use anticonvulsants, antihistamines, sedatives, and/or anxiolytics; have orthodontic appliances; have a history of or current presence of neoplasms in the head and neck region; or are allergic to any component of the products used in the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe a decrease in the level of dental pain in response to mechanical and thermal stimuli, as assessed by the Visual Analog Scale, in pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactFelipe Rafael da Cunha Araújo
Faculdade de Odontologia de Bauru - Universidade de São Paulo
Outcome results
None listed