Status:
COMPLETED
Non-carious Cervical Lesions and Treatments
Lead Sponsor:
University of Sao Paulo
Conditions:
Tooth Sensitivity
Eligibility:
All Genders
18-60 years
Phase:
NA
Brief Summary
This study will compare clinically the efficacy, time to action and duration of different treatments for patients with non-carious cervical lesions (NCCLs) that caused dentin hypersensitivity (DH).
Detailed Description
This study will compare clinically the efficacy, time to action and duration of different treatments for patients with non-carious cervical lesions (NCCLs) that caused dentin hypersensitivity (DH). Ca...
Eligibility Criteria
Inclusion
- \- (a) male or female between 18 to 60 years old; (b) good general (no diseases that could interfere in the results) and oral health (no alterations in hard or soft tissues); (c) a minimum of 24 permanent teeth; (d) presence of non-carious cervical lesion; and (e) compliment of cervical dentin hypersensitivity
Exclusion
- (a) chronic analgesic or anti-inflammatory therapy; (b) orthodontic treatment or dental prosthesis; (c) desensitization therapy in the preceding 3 months; (d) alimentary disorder or acid diet; and (e) pregnant or lactating women.
Key Trial Info
Start Date :
August 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 10 2018
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT03403088
Start Date
August 1 2017
End Date
October 10 2018
Last Update
October 11 2018
Active Locations (1)
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1
University of Sao Paulo -Ribeirao Preto Campus
Ribeirão Preto, São Paulo, Brazil, 14040904