Extraction of impacted third molars.
Conditions
Interventions
A randomized, controlled, double-blind, clinical trial. 500 patients undergoing treatment at the Dental Specialty Center for the removal of impacted lower third molars will participate in the study.
A
other
E02.594.540
Sponsors
Universidade Nove de Julho
Universidade Nove de Julho
Eligibility
Inclusion criteria
Inclusion criteria: Patients who need to perform removal of impacted third molars and to accept part of the study as informed consent and informed.
Exclusion criteria
Exclusion criteria: Systemic diseases, chronic pain or neurological and psychiatric disorders. Being a smoker. Being using anti-inflammatories, analgesics or bisphosphonates in the past 15 days have provided the framework of pericoronitis in the last month. Being pregnant. Being breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare, using visual analogue scale (VAS), pain symptoms due to removal of impacted lower third molars in patients who received laser irradiation postoperatively and in patients who did not receive laser irradiation. Compare, through three facial measurements pre and post-operative swelling due to surgery in patients who received laser irradiation postoperatively and in patients who did not receive laser irradiation. Compare, through the measurement of mouth opening, muscle spasm due to surgery in patients who received laser irradiation postoperatively and in patients who did not receive laser irradiation. | — |
Countries
Brazil
Contacts
Public ContactSimone Sierra
Universidade Nove de Julho
Outcome results
None listed