Pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Will be included in the study, 24 patients aged between 18 and 30 years and without impairment of general health according to medical history (healthy) and physical examination, who agree to participate in the study. Through clinical and radiographic examination, patients with indication for bilateral extraction of mandibular third molars, asymptomatic and in class IIB position, according to the Pell & Gregory classification, will be selected.
Exclusion criteria
Exclusion criteria: Exclusion criteria will be considered: (I) history of use of any type of analgesic, anti-inflammatory and antibiotic medication in the 15 days prior to the beginning of the surgical procedure; (II) history of hypersensitivity to drugs, substances or materials used in this experiment; (III) pregnancy or lactation; (IV) pericoronitis or other local infection within 15 days prior to the surgical procedure; (V) and people with a history of acute or chronic systemic disease, such as hypertension or diabetes, for example.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is believed that there is a great possibility of reducing the perception of pain, edema, trismus and the use and number of medications used in the postoperative period of tooth extraction surgeries with the use of the proposed protocols, given the possibility of minimizing the related adverse effects inflammation caused by the surgical procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| In addition, an improvement in quality of life is expected in the postoperative period of third molar extraction. | — |
Countries
Brazil
Contacts
Universidade Federal de Uberlândia