Anxiety Disorders
Conditions
Interventions
Research participants will be included in two groups, each group will contain 30 volunteers. In group 1, patients will receive thirty minutes before surgery, the protocol:
Dexamethasone 8 mg intramusc
K01.0
Sponsors
Universidade Federal de Sergipe
Universidade Federal de Sergipe
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients who after diagnosis are indicated for bilateral extraction of asymptomatic third molars and in similar surgical positions and difficulties, analyzed through panoramic radiographs.
Exclusion criteria
Exclusion criteria: Patients under 18 years of age; patients classified as ASA III or IV; history of use of pain or anxiety medication in the 15 days prior to the start of the research; history of hypersensitivity to drugs, substances, or materials used in this experiment; pregnancy or lactation; previous history of pericoronitis, as it changes the pain sensitivity of the patient; systemic diseases using control medication; odontophobia; very anxious patients, using as a parameter for classification the Corah scale; mental disability.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find pain control after third molar surgery, verified by the method of the visual analogue scale that is expressed in a 10 cm line, containing the indication without pain in the left limit and unbearable pain in the right. The distance between the start of the appointment, indicated by no pain, to the appointment made by the research volunteers at EVA will be measured. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactAnne Gercina
Outcome results
None listed