Effects of Photobiomodulation Conditioning in Impacted Third Molars
NCT ID: NCT05344222
Last Updated: 2022-04-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
62 participants
INTERVENTIONAL
2021-07-01
2022-03-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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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.
Infrared LED
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.
Sham Photobiomodulation
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.
Similar device - Infrared ED
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.
Interventions
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Infrared LED
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.
Similar device - Infrared ED
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.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
60 Years
ALL
Yes
Sponsors
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University of Nove de Julho
OTHER
Responsible Party
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Anna Carolina Ratto Tempestini Horliana
Clinical professor
Principal Investigators
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ERIKA MELLO
Role: PRINCIPAL_INVESTIGATOR
University of Nove de Julho
Locations
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University of Nove de Julho (UNINOVE)
São Paulo, , Brazil
Countries
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References
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Related Links
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Roochi MM, Heidar H, Kordi S, Bahrami N. Efficacy of low level laser for prevention of pain and trismus after impacted mandibular third molar surgery. J Craniomaxillofacial Res. Published online May 16, 2017:284-288. Accessed January 21, 2021
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Other Identifiers
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HALIURO
Identifier Type: -
Identifier Source: org_study_id
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