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Clinical Trials/RBR-25f7sc
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.

Registry
who.int
Start Date
September 14, 2020
End Date
TBD
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
niversidade Luterana do Brasil

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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