Postoperative Pain
Conditions
Interventions
The study will be prospective, double blind, randomized,two groups, split-mouth type(the same participant will have both control medication and test medication), in which 20 patients with indication f
Sponsors
Universidade Estadual do Rio de Janeiro
Universidade Estadual do Rio de Janeiro
Eligibility
Age
16 Years to 30 Years
Inclusion criteria
Inclusion criteria: ASA I, according to American Society of Anesthesiology (ASA) criteria; with the need for bilateral extraction of lower third molars; dental elements that present similarity of positioning; Class 1 and 2 impacted teeth and A and B by Pell and Gregory classifications; non-smokers
Exclusion criteria
Exclusion criteria: History of pericoronitis in the lower third molar region; cystic lesion involving the lower third molar; allergy to any medication prescribed in the postoperative period; any systemic or autoimmune disease; use of other concomitant medications; pregnant patients; lactose intolerant or allergic; surgeries exceeding 40 minutes in duration; smokers volunteers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to verify that there are no differences in pain control between the test group and the control group through the visual and numerical analog scale and patient report, in the two surgical moments. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactIolanda Lemos
Universidade Estadual do Rio de Janeiro
Outcome results
None listed