Effect of different protocols in the treatment of tooth sensitivity
Not Applicable
Recruiting
- Conditions
- Dentin ErosionDentin Sensitivity
- Registration Number
- RBR-5nw4zp
- Lead Sponsor
- niversidade Estadual Paulista - FOA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
For the in vivo study, patients will be selected who:Age between 20 and 70 years old; regardless of sex; Good health; with no history of allergies to dental products; Presence of at least 1 non-cavitated root exposures or with the beginning of cavitation (without need for restoration), which is sensitive to the jet from a distance of 10 cm.
Exclusion Criteria
For in vivo study:Pregnant, lactating or smokers; Presence of active caries lesions; Use of desensitizing agents in the last 6 months; Active and untreated periodontal disease; Use of orthodontic appliance or removable partial denture with clamp on the tooth to be evaluated;Severe bruxism, with more than 50% wear
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expect to find an innovative and effective clinical protocol,verified through tooth sensitivity and analysis, for treatment to dentin hypersensitivity. <br><br>
- Secondary Outcome Measures
Name Time Method Secondary outcomes are not expected<br><br>