Pain
Conditions
Interventions
A randomized, controlled, two-arm, double-blind clinical trial will be performed. 30 patients will be selected with indication for extraction of the 2 lower third molars (total of 60 extractions). All
Sponsors
Universidade de Pernambuco
Faculdade de Odontologia da Universidade de Pernambuco
Eligibility
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: age between 18 to 30 years; present surgical site without current signs and symptoms of infection; present mandibular third molars in similar positions and with indication for extraction
Exclusion criteria
Exclusion criteria: history of pregnancy or lactation; history of allergy to any medication used in the experiment; not participating in all phases of the proposed research; systemic disease; making use of medications that interfere with the procedure on the day or week prior to the survey
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to evaluate whether healing by second intention of the relaxing incision promotes a lower degree of edema in the postoperative period of third molar extraction. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to evaluate whether healing by second intention of the relaxing incision promotes a lower degree of trismus in the postoperative period of third molar extraction.;It is expected to evaluate whether healing by second intention of the relaxing incision promotes a lower degree of pain in the postoperative period of third molar extraction. | — |
Countries
Brazil
Contacts
Public ContactÉwerton Rocha Rodrigues
Faculdade de Odontologia da Universidade de Pernambuco
Outcome results
None listed