Dentin hypersensitivity
Conditions
Interventions
This is a randomized controlled double blind clinical trial. The present study will be carried out at the dental clinics of ULBRA Canoas and will include a sample of 50 individuals who will be selecte
Drug
Device
E02.594
Sponsors
Universidade Luterana do Brasil
Universidade Luterana do Brasil
Eligibility
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Individuals 18 to 75 years of age. Both genders Clinically healthy individuals Availability to participate in the entire study Sign the terms of free consent Present hypersensitivity in non-adjacent teeth Clear clinical presence of changes such as aberration, distress and erosion in anterior and / or molar teeth. Response to the air jet stimulus for one second in the cervical region, as defined by the score 2 or 3 on the Schiff scale for sensitivity to the air stimulus. Have good oral hygiene
Exclusion criteria
Exclusion criteria: Individuals with joys at the product being tested. Individuals with clinical presence of pathologies recorded in the soft tissues. Individuals undergoing chemotherapy and radiation therapy. Individuals with gingivitis and / or periodontitis. Individuals who will start taking anticonvulsants, antihistamines, antidepressants, sedatives, tranquilizers, anti-inflammatory or analgesic drugs up to one month before the start of the study or who will start taking it during the study. Individuals took antibiotics three months before the study. Individuals participating in another study Pregnant or breastfeeding women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of dentin hypersensitivity in adult patients using 8% arginine-based desensitizing dentifrice and as a supporting treatment use of 320-360 nm low power laser, verified using the Schiff scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactEduardo Reston
Universidade Luterana do Brasil
Outcome results
None listed