Anti-Inflammatory Agents
Conditions
Interventions
This study is a randomized, 3-arm, triple-blind clinical trial. 29 patients and 36 teeth were selected (taking into account that each patient could have two teeth allocated to two different groups) wh
Sponsors
Universidade Santo Amaro
Universidade Santo Amaro
Eligibility
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: They presented good systemic health conditions (ASA I); were between 18 and 35 years of age of both sexes; were indicated for extraction of the 38 and/or 48 impacted or semi-impacted dental elements, requiring a total mucoperiosteal flap and osteotomy
Exclusion criteria
Exclusion criteria: Patients who did not meet these inclusion criteria; who had any local inflammatory or infectious condition that would contraindicate tooth extraction; any type of hypersensitivity reaction to the medicinal substances that were used in the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: It was hoped that the use of dexamethasone would promote lower or equal values to the non-steroidal anti-inflammatory drugs Ibuprofen and Ketorolac, with regard to the parameters of pain.;Outcomes found 1: As an outcome, it was observed that the ketorolac was the one that promoted the best values for the parameters of analgesia | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: It was expected to observe that the use of dexamethasone could promote lower or equal values to the non-steroidal anti-inflammatory drugs Ibuprofen and Ketorolac, regarding the parameters edema and trismus;Outcome found 2: As a secondary outcome, it was observed that the NSAID ketorolac was the one that promoted better values for the parameters edema and trismus | — |
Countries
Brazil
Contacts
Public ContactGustavo Momesso
Universidade Santo Amaro
Outcome results
None listed