Dental hypomineralization Dentin Hypersensitivity
Conditions
Interventions
This is a prospective longitudinal clinical study, non-randomized, single-arm and non-blinded, involving 35 participants allocated to a single intervention group, aiming to evaluate the effect of Refi
Sponsors
Universidade de São Paulo
Faculdade de Odontologia Bauru
Eligibility
Age
6 Years to 16 Years
Inclusion criteria
Inclusion criteria: Children and adolescents aged 6 to 16 years; presence of molar incisor hypomineralization; presence of dentin hypersensitivity; parents or guardians who provided informed consent; participants who provided assent
Exclusion criteria
Exclusion criteria: Patients with enamel defects not related to molar incisor hypomineralization; presence of extensive carious lesions in evaluated teeth; recent use of desensitizing agents; systemic conditions that may interfere with dentin hypersensitivity; uncooperative patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of dental hypersensitivity in teeth affected by hypomineralization (MIH/DMH/HSPM), assessed using the Visual Analog Scale (VAS) and the Schiff Cold Air Sensitivity Scale (SCASS), after application of the Refix/Booster system. | — |
Secondary
| Measure | Time frame |
|---|---|
| Impact of the intervention on oral health-related quality of life, assessed using the Child Perceptions Questionnaire (CPQ) during the follow-up period. | — |
Countries
BR
Contacts
Public ContactPriscila Gregorio
Faculdade de Odontologia Bauru
Outcome results
None listed