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Effect of Low-level Laser Therapy on Post-bleaching Sensitivity and Color Change

Not Applicable
Completed
Conditions
Low-level Laser Therapy
Dentin Sensitivity
Clinical Trial
Tooth Bleaching
Interventions
Radiation: Low-lever laser
Other: Tooth bleaching
Other: Placebo
Registration Number
NCT03514290
Lead Sponsor
Universidade Federal do Para
Brief Summary

Objective: The objective of this clinical study was to evaluate low-level laser (LLL) therapy in tooth sensitivity and in effecting color change after in-officer bleaching treatment across three weeks of treatment.

Methods: Twenty-one volunteers were evaluated through the split-mouth model, so that the right and left maxillary/mandibular quadrants were randomized and allocated to one of two groups: GPLACEBO - the laser tip was positioned without the emission of light (placebo effect) + tooth bleaching with 35% hydrogen peroxide (HP); GLASER - treated with LLL + tooth bleaching with 35% HP. To assess tooth sensitivity, a modified visual analogue scale (VAS) was used after an evaporative stimulus (stimulated pain) and a daily pain questionnaire (unstimulated pain) was also applied. A spectrophotometer was used to measure the color. Three bleaching sessions were performed, with intervals of 7 days. Sensitivity results were tested using Friedman test for intra-group evaluation and Wilcoxon test for inter-group evaluation and ANOVA for color change.

Detailed Description

Twenty-one volunteers were evaluated through the split-mouth model, so that the right and left maxillary/mandibular quadrants were randomized and allocated to one of two groups: GPLACEBO - the laser tip was positioned without the emission of light (placebo effect) + tooth bleaching with 35% hydrogen peroxide (HP); GLASER - treated with LLL + tooth bleaching with 35% HP. To assess tooth sensitivity, a modified visual analogue scale (VAS) was used after an evaporative stimulus (stimulated pain) and a daily pain questionnaire (unstimulated pain) was also applied. A spectrophotometer was used to measure the color. Three bleaching sessions were performed, with intervals of 7 days.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
21
Inclusion Criteria
  • Do not have previous dental sensitivity
  • The canine had to be shade A2 or darker.
Exclusion Criteria
  • Enamel hypoplasia
  • Gingival recession
  • Dentin exposure
  • Visible cracks on buccal enamel
  • Pulpitis

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
GLASERTooth bleachingtreated with Low-lever laser + tooth bleaching with 35% hydrogen peroxide (HP).
GPLACEBOTooth bleachingthe laser tip was positioned without the emission of light (placebo effect) + tooth bleaching with 35% hydrogen peroxide (HP).
GPLACEBOPlacebothe laser tip was positioned without the emission of light (placebo effect) + tooth bleaching with 35% hydrogen peroxide (HP).
GLASERLow-lever lasertreated with Low-lever laser + tooth bleaching with 35% hydrogen peroxide (HP).
Primary Outcome Measures
NameTimeMethod
Dental sensitivity induced by office bleachingchange in baseline sensitivity at the 3rd bleaching session

Evaporative stimulus (stimulated pain) using air jet from a triple syringe and a daily pain questionnaire (unstimulated pain). Both methods were associated with a modified visual analogue scale was used: 0 (pain absent); 1 (mild pain); 2 (moderate pain) and 3 (severe pain).

Secondary Outcome Measures
NameTimeMethod
Color change promoted by tooth bleachingchange in baseline color at the 3rd bleaching session

Spectrophotometer was used to measure the color

Trial Locations

Locations (1)

Federal University of Pará

🇧🇷

Belém, PA, Brazil

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