Effects of Photobiomodulation Conditioning in Impacted Third Molars
Impacted Third Molar Tooth
About this trial
This is an interventional prevention trial for Impacted Third Molar Tooth
Eligibility Criteria
Inclusion Criteria:
- male and female adults (18 years of age or older)
- no tumors in the oral region,
- not having undergone psychiatric treatment in the previous year,
- good general health,
- satisfactory oral hygiene,
- impacted mandibular third molar
- signed statement of informed consent.
Exclusion Criteria:
- habitual use of analgesic or anti-inflammatory medication for other comorbidities,
- undergoing neurological/psychiatric treatment,
- teeth with lesions to be treated in the same hemi-arch as the tooth to be removed,
- systemic disease,
- current smoking habit,
- pericoronitis in the previous 30 days,
- pregnant or nursing women,
- poor oral hygiene,
- photosensitivity disorder,
- tumor in the oral region,
- heart disease,
- diabetes,
- blood dyscrasia,
- chemical dependency,
- allergy to medications used in the study,
- ankylosis of the temporomandibular joint
- intraoperative complications with surgery time exceeding 90 minutes.
Sites / Locations
- University of Nove de Julho (UNINOVE)
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Photobiomodulation
Sham Photobiomodulation
The participants in the active photobiomodulation group will be irradiated with infrared LED at a wavelength of 850 nm perpendicular to the surface of the skin in gentle stationary contact at three extraoral points. Treatment will be administered one hour prior to the surgical procedure as well as 48 hours and seven days (removal of sutures) after the first irradiation.
For the participants in the sham group, a device with a similar appearance will be used that did not emit radiation. Treatment will be administered one hour prior to the surgical procedure as well as 48 hours and seven days (removal of sutures) after the first irradiation.