clinical trial
Conditions
Interventions
BioMin F Group: 20 participants with one tooth with dentin hypersensitivity greater than or equal to 4 on the visual analog scale after an evaporative stimulus and after a tactile stimulus. Participan
Sponsors
Faculdade de Odontologia de Bauru
Faculdade de Odontologia de Bauru
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Volunters older than 18 years old; with one tooth with dentin hypersensitivity igual to or higher than 4.
Exclusion criteria
Exclusion criteria: Patients with active caries lesions; defective restorations on selected teeth; structural loss of dentin that requires restorative or periodontal treatment; who has used any professional desensitizing agent in the past 6 months; use of some desensitizing toothpaste in the last 3 months; who uses anti-inflammatory medicine during the study period; patients using orthodontic appliances; smokers; pregnant women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The reduction of dentin hypersensitivity verified immediately after the first use of the product, after 1 month, 3 months and 6 months will be evaluated by the use of the visual analog scale associated with evaporative and tactile stimuli in sensitive teeth, and its influence on the related quality of life oral health measured by changing the score of the OHIP-14 questionnaire, and the differences will be assessed based on the finding of a variation of at least 5% in the measurements between periods. | — |
Countries
Brazil
Contacts
Public ContactVictor Mosquim
Outcome results
None listed