Dentin Sensitivity
Conditions
Interventions
A randomized, blinded, split-mouth clinical trial will be conducted to investigate the effects of potassium oxalate gel (Oxa-gel BF) and a gel made with a commercial type of bioglass (45S5) in the tre
Sponsors
Programa de Pós-Graduação em Odontologia da Universidade Federal do Ceará
Universidade Federal do Ceará
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years of age; both genders - male and female; good oral hygiene; without periodontal disease or dysfunctional habits; who have at least one cervical lesion in the quadrant diagnosed as moderate or severe hypersensitivity
Exclusion criteria
Exclusion criteria: Desensitizing treatment in the last six months; history of chronic use of medications such as antidepressants, antihistamines, nonsteroidal anti-inflammatory drugs, anticonvulsants or sedatives; history of allergies to dental products; pregnant or lactating patients; orthodontic appliances; the selected teeth should not have pulpitis, crowns, abutments, extensive or defective restorations on the vestibular surface, nor cracks in the enamel, fractures or cavities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effect of bioglass on the control of dentin hypersensitivity (DH), through a blind clinical trial | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effect of bioglass on the control of HD immediately after;To evaluate the effect of bioglass on the control of HD after 3 months;To evaluate the effect of bioglass on the control of HD after 6 months;To evaluate the influence of treatments for the control of HD on the quality of life related to oral health | — |
Countries
Brazil
Contacts
Public ContactAna Karolaynne Rodrigues
Universidade Federal do Ceará
Outcome results
None listed