Dentin Sensitivity
Conditions
Interventions
The present study aims to be a double-blind randomized clinical trial (the patient will be blinded by means of completely dark glasses and the study evaluator, who will not know which of the technique
Sponsors
Universidade Estadual do Oeste do Paraná
Universidade Estadual do Oeste do Paraná
Eligibility
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Patients of both sexes will be included in the study; aged between 18 and 35 years; with all vital anterior teeth; never whitened or restored; with periodontal health; no history of spontaneous dental pain; that do not use toothpaste with desensitizing properties; with grade 1 to 3 dentin sensitivity; willing to return for future evaluations during the research period
Exclusion criteria
Exclusion criteria: Patients with missing anterior teeth will be excluded from the study; affected by caries lesions; with the presence of recession; with some type of restorative or prosthetic treatment; or who use fixed orthodontic appliances; patients with bruxism or visible enamel cracks; patients with a history of periodontal disease or active periodontal disease; patients with a history of dental hypersensitivity; patients with tooth color changes due to fluorosis or tetracycline; patients who use many medications; and pregnant or lactating patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Demonstrate the reduction of tooth sensitivity through ozone therapy in patients with hypersensitivity. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate color change during ozone therapy treatment;To compare the pain perception of the gold standard of whitening with ozone therapy in dentin sensitivity;Determine whitening protocol in patients with dentin sensitivity using ozone therapy | — |
Countries
Brazil
Contacts
Public ContactVeridiana Camilotti
Universidade Estadual do Oeste do Paraná
Outcome results
None listed