Fluoride
Conditions
Interventions
A randomized, crossover, double-blind clinical study (with regard to participants and researchers) was carried out. Sixteen adults aged between 20 and 32 years participated in this study, eight men an
Sponsors
Universidade Federal do Piauí
Universidade Federal do Piauí
Eligibility
Age
20 Years to 32 Years
Inclusion criteria
Inclusion criteria: Favorable oral and systemic conditions; availability to participate in the research and comply with the determinations required by the experimental protocol; normal salivary flow; both genders; from 20 to 32 years old
Exclusion criteria
Exclusion criteria: use of medications that alter salivary flow; fluoride supplements; smokers; presence of active carious lesion; periodontal disease; fixed orthodontic appliance; allergy or sensitivity to the ingredients of the study varnishes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determination of salivary fluoride concentration in saliva. It is expected to observe an increase in the salivary concentration of fluoride after the application of fluoride varnishes in the initial times after application with a subsequent decline. | — |
Secondary
| Measure | Time frame |
|---|---|
| Calculate the area under the curve of fluoride concentration in saliva over time. It is expected that the varnishes present a similar area under the curve value and that these values are greater when the fluoride dentifrice is associated with the varnish. | — |
Countries
Brazil
Contacts
Public ContactGlauber Vale
Universidade Federal do Piauí
Outcome results
None listed