Dentin Sensitivity
Conditions
Interventions
No drugs. A 21-day double-blind, parallel, prospective, equivalence controlled clinical trial will be performed. 60 patients will be recruited as they seek treatment at university clinics. Patients wi
Sponsors
Andres Felipe felipe Millan Cardenas
Centro Universitário de Maranhão - UNICEUMA
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Good oral and general health; be at least 18 years of age; probing depth less than 3 millimeters, dentin sensitivity; have at least 2 teeth and a maximum of 4 teeth with non-carious cervical lesions
Exclusion criteria
Exclusion criteria: Patients with advanced periodontal disease; severe or chronic periodontitis; bruxism; Pregnant or lactating participants; participants in chronic use of anti-inflammatory, analgesic or psychotropic drugs, patients with dental fractures, or with unsatisfactory restorations or deep caries or who use fixed, removable or total partial dentures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in the level of dentin hypersensitivity, determined by Visual Analogue Scale and Shiff scale immediately, after 3, 7, 14 and 21 days of treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactAndres;Fabiana Cardenas;de Siqueira
Universidade CEUMA;Universidade CEUMA
Outcome results
None listed