Pain, Postoperative
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. A total of 102 people who meet the eligibility criteria will be randomized using the Randomizer software. Researchers and partici
Sponsors
Universidade Federal do Paraná - UFPR
Universidade Federal do Paraná - UFPR
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: This study may include adults over 18 years of age of both sexes who require third molar extraction
Exclusion criteria
Exclusion criteria: Patients under 18 years of age, with a history of using pain or anxiety medications in the 15 days prior to the study, with a history of hypersensitivity to medications, substances or materials used in this experiment, pregnant or lactating women. Patients with general health problems will not be eligible for participation in the study, as well as immunosuppressed patients, people who use anticoagulant or antiplatelet therapy, HIV patients, diabetes mellitus, and patients who are undergoing chemotherapy, as these conditions may interfere with the study results.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe pain relief or control in patients undergoing surgery for third molar extraction (wisdom tooth) shortly after surgery and in the three days after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of aspects associated with pain such as anxiety, stress, trismus, edema and surgical discomfort are expected | — |
Countries
Brazil
Contacts
Public ContactVanessa Lejeune
Universidade Federal do Paraná - UFPR
Outcome results
None listed