Tooth, Unerupted
Conditions
Interventions
This is a split-mouth, double-blind, randomized clinical study. The sample will consist of 40 individuals between 18 and 45 years old, with indication of bilateral extraction of the lower third molars
each group consisted of 40 procedures. In order to ensure adequate randomization, brown and opaque envelopes were used to store information regarding the drug combinations intended for the groups (Nim
Sponsors
Universidade Federal de Pernambuco
Universidade Federal de Pernambuco
Eligibility
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Adults aged between 18 and 45, of both sexes; in ASA in group I; with indication of bilateral extraction of lower third molars; The right and left lower third molars of the included individuals must present the same degree of inclusion according to the classification of Pell and Gregory (1933) determined by means of panoramic radiography or cone beam computed tomography
Exclusion criteria
Exclusion criteria: Patients who are allergic to NSAIDs (nimesulide or etoricoxib) and/or corticosteroids (dexamethasone); signs of infection at the surgical site; chronic users of analgesics and/or anti-inflammatories; smokers; pregnant or breastfeeding women; patients who did not fit into the surgical or anesthetic planning and patients who withdrew from participating in the research at any time
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate which medication protocol allowed for greater control of postoperative pain, reducing the need for the use of analgesic medications in the postoperative period | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to observe which medication protocol made it possible to reduce the negative impacts of the surgical trauma caused | — |
Countries
Brazil
Contacts
Public ContactPriscilla Pinto
Universidade Federal de Pernambuco
Outcome results
None listed