Dentofacial anomaly, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Individuals indicated to undergo bimaxillary orthognathic surgery with genioplasty; removal of third molars at least 6 months before surgery; regardless of gender and race; age group above 18 years; Signature of the Informed Consent Form (ICF).
Exclusion criteria
Exclusion criteria: Individuals submitted to monomaxillary surgery will be excluded; patients under 18 years of age; individuals with temporomandibular joint dysfunction; rupture of the inferior alveolar nerve during the surgical procedure; undesirable fractures; mandibular surgery with execution time above 2:30 h; deficient mandibular fixation; allergy to standardized anti-inflammatory drugs; postoperative infection; individuals who did not cooperate with PBMT therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate whether 940 nm laser photobiomodulation therapy in the postoperative period of orthognathic surgery will bring benefits to the patient in the postoperative period. | — |
Secondary
| Measure | Time frame |
|---|---|
| The 940 nm laser photobiomodulation therapy in the postoperative period of orthognathic surgery is expected to decrease the amount of edema in the postoperative period.;The 940 nm laser photobiomodulation therapy in the postoperative period of orthognathic surgery is expected to decrease the amount of pain in the postoperative period.;The 940 nm laser photobiomodulation therapy in the postoperative period of orthognathic surgery is expected to decrease the amount of patient paraesthesia in the postoperative period.;The 940 nm laser photobiomodulation therapy in the postoperative period of orthognathic surgery is expected to decrease the amount of patient trismus in the postoperative period. | — |
Countries
Brazil
Contacts
Faculdade de Odontologia da Universidade de São Paulo