Dentin Sensitivity Oral Health
Conditions
Interventions
This is a randomized, double-blinded, controlled clinical study that aims to evaluate the in vivo efficacy of Brazilian red propolis (BRP) toothpaste in the prevention and control of dentin hypersensi
s reaction is assessed using the Schiff Scale, and the VAS (Visual Analogue Scale) will also be applied.
Sponsors
Instituto Leão Sampaio de ensino universitário
Universidade Federal do Ceará
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age 18 or older; Presence of dentin hypersensitivity; Teeth (incisors, canines, premolars, or first molars) with a positive response to evaporative cold air stimulus on the Schiff Sensitivity Scale.
Exclusion criteria
Exclusion criteria: Pregnant women; Patients who underwent teeth whitening up to 8 weeks before the start of the study; Patients with a history of allergy to the components of the study material; Use of toothpaste or other type of desensitizing agent in the 30 days prior to the study; Teeth with mobility; Teeth with deep and defective restorations; Teeth with caries, fissures, fractures or any sign of pulpitis; Teeth with a history of trauma; Teeth used as abutments for removable partial dentures; History of allergy to propolis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the ecreased tooth sensitivity | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected an improvement in quality of life | — |
Countries
BR
Contacts
Public ContactThiago Bezerra Leite
Universidade Federal do Ceará
Outcome results
None listed