Dentin-Bonding Agents
Conditions
Interventions
This research is a randomized, split-mouth, double-blind clinical study. Twenty patients with an indication for third molar extraction and aged over 18 years will be selected to receive two restorati
Sponsors
Universidade Federal do Mato Grosso do Sul
Universidade Federal do Mato Grosso do Sul
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Volunteer aged 18 or over; both genders; present good oral health conditions, without severe or chronic periodontal disease; presence of at least two third molars with indicated extraction
Exclusion criteria
Exclusion criteria: Presence of acute pain related to third molars; continuous use of analgesics and anti-inflammatories; history of known allergy to the restorative materials to be used; difficulty accessing third molars due to anatomical or surgical factors; presence of temporomandibular disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the effect of moisture control in dentin on the dentin/resin interface using a conventional adhesive system | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find a practical and effective clinical protocol for composite resin restorations with less tooth sensitivity, evaluated with a Visual Analogue Scale, spontaneously and stimulated in 24 hours, 7 days, and 15 days after the restorative procedure. | — |
Countries
Brazil
Contacts
Public ContactAndrea Freire
Universidade Federal do Mato Grosso do Sul
Outcome results
None listed