Evaluation of desensitizing protocols in reduction of teeth hypersensitivity level
- Conditions
- Stomatognathic diseases, dentin sensitivity, tooth erosion, tooth abrasionC07.793.266C07.793.818.500C07.793.818.124
- Registration Number
- RBR-4752vs
- Lead Sponsor
- Faculdade de Odontologia da Universidade Federal de Uberlândia - FOUF
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Healthy individuals of both sexes who are interested in the treatment of Dentin Hypersensitivity; Agree to participate and sign the informed consent form (TCLE); Patients with all teeth in their mouth; Patients with at least three teeth with Dentin Hypersensitivity in different quadrants.
Presence of dentin hypersensitivity caused due to the presence of caries or unsatisfactory restorations; Patients in orthodontic or periodontal treatment; Patients performing dental whitening; Presence of spontaneous pain in the tooth with dentin hypersensitivity, characterizing pulpitis; Presence of periodontal disease; Unsatisfactory oral hygiene; Use of extensive prostheses; Patients with severe bruxism and loss of vertical dimension; Patients with uncontrolled gastroesophageal reflux disease; Patients with uncontrolled systemic and / or psychological diseases; Pregnancy and smokers.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in dentin hypersensitivity in patients<br>submitted to different treatment protocols in a a 24 weeks follow-up. The evaluation will be carried out by visual analogy scale of pain from the observation of a range of at least 30% in the pre and post intervention measurements.
- Secondary Outcome Measures
Name Time Method To determine an effective treatment protocol for reduction in dentin hypersensitivity, regarding the number of application sessions and the type of agent used.