RBR-25f7sc
Not yet recruiting
未知
Clinical evaluation on the effectiveness of reducing dental hypersensitivity in patients using 8% arginine-based dentifrices and a 320-360 nm laser. Parallel Randomized Clinical Trial
niversidade Luterana do Brasil0 sitesSeptember 14, 2020
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Dentin hypersensitivity
- Sponsor
- niversidade Luterana do Brasil
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility 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
- •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.
Outcomes
Primary Outcomes
Not specified
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