Stomatognathic diseases, tooth abrasion, dentin sensitivity, tooth erosion
Conditions
Interventions
This study refers to a clinical follow-up, in which 32 subjects with dentin hypersensitivity in less than two teeth in different quadrants receive two types of desensitization protocols. Group 1: Prot
Drug
Sponsors
Hospital Odontológico da Universidade Federal de Uberlândia
Universidade Federal de Uberlândia
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: The criteria for inclusion of the patients will be: healthy individuals 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 two teeth with Dentin Hypersensitivity in different quadrants.
Exclusion criteria
Exclusion criteria: The criteria for exclusion of patients will be: 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in dentin hypersensitivity in patients submitted to different concentration with twotypes of potassiun oxalate in 3 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
| Measure | Time frame |
|---|---|
| To determine an effective treatment protocol for reduction in dentin hypersensitivity, regarding the desensitizing agent concentration.The effectiveness evaluation will be carried out by visual analogy scale. | — |
Countries
Brazil
Contacts
Public ContactPaulo Soares
Faculdade de Odontologia da Universidade Federal de Uberlândia - FOUFU
Outcome results
None listed