MedPath

Photobiomodulation and Root Resorption

Not Applicable
Completed
Conditions
Orthodontic Tooth Movement
Orthodontic Appliance Complication
Orthodontic Pathological Resorption of External Root
Interventions
Device: Laser
Device: light-emitting diode (LED)
Device: Placebo
Registration Number
NCT04044989
Lead Sponsor
University of Gaziantep
Brief Summary

Objectives: The aim of this study is to investigate the effect of photobiomodulation therapies on root resorption compared with the placebo group. Materials and Methods: 30 patients, who were admitted to the ............. University Faculty of Dentistry Orthodontics Department for treatment, with an indication of upper right 1st premolar tooth extraction was included. Before the individuals' orthodontic treatment, 0.022 slot MBT brackets and tubes were placed on the maxillary 1st premolar and molar. A 150g buccal tipping force was applied to the 1st premolar. Individuals were then randomly divided into 3 groups. For the first group; laser application was performed with a 810 nm GaAlAs laser device at 0,3,7,14,21 and 28 days to 8 J/cm2. Second group; an LED application according to the manufacturer's instructions with a 850 nm wavelength and 20 mW/cm2 output power for 10 minutes per day during the experiment. Third group; a placebo therapy was completed whereby a laser device that did not make active pulses was used. At the end of four weeks, the amount of root surface resorption was compared using micro-CT imaging after the extraction of the teeth.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • No history of orthodontic treatment
  • No systemic disease or craniofacial anomaly
  • No dental trauma and tooth with root resorption
  • Having good oral hygiene
  • No periodontal disease (no more than 3mm pocket)
  • No restored or endodontically untreated upper right 1st premolar teeth
  • Having the maxillary right 1st premolar tooth extraction indication of orthodontic treatment
Exclusion Criteria
  • Problems in patient compliance
  • Inadequate oral hygiene
  • Development of any medical problem making orthodontic treatment contraindicated during the study period

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Root resorption (local)PlaceboThe resorption cavities on the root surface (palatal, buccal, distal and mesial root surfaces) were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Root resorption (total)LaserThe resorption cavities on the root surface were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Root resorption (total)PlaceboThe resorption cavities on the root surface were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Root resorption (local)LaserThe resorption cavities on the root surface (palatal, buccal, distal and mesial root surfaces) were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Root resorption (total)light-emitting diode (LED)The resorption cavities on the root surface were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Root resorption (local)light-emitting diode (LED)The resorption cavities on the root surface (palatal, buccal, distal and mesial root surfaces) were determined and the volumes of the cavities were measured in CTAn software (micro-CT).
Primary Outcome Measures
NameTimeMethod
Root Resorptionthrough study completion, an average of 4 weeks

Crater volume measurement

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Gaziantep University

🇹🇷

Gaziantep, Turkey

© Copyright 2025. All Rights Reserved by MedPath