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Study of the therapies for dentin hypersensitivity.

Not Applicable
Conditions
Tooth wear,Dentine hypersensitivity,Dental Materials
C07.793.818
Registration Number
RBR-4x2957
Lead Sponsor
niversidade Federal do Piauí
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

The volunteers: they will be included with age 18 years or older, enrolled in the clinics of dentistry UFPI having at least 20 dental elements.
Non-carious lesions: at least four lesions whose sensitivity is classified by the patient for moderate to severe after administration of a air, and tooth wear between 2 and 4. These teeth must have an antagonist tooth.

Exclusion Criteria

The patient: will be excluded people who have made periodontal treatment and/or hypersensitivity treatment in the last six months, patients with bruxism in the active phase.
Non-carious lesions: teeth with very deep lesions, when a ruber dam isolation is not possible and those that have been previously restored.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It is expected that one of the interventions is more effective in controlling dentinal hypersensitivity not carious lesions. The outcome will be assessed by analyzing the presence of pain induce by an air jet against the site where the intervention was carried out.
Secondary Outcome Measures
NameTimeMethod
It is expected that all interventions are effective up to 6 months of intervention.
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