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NCT Number: NCT03089216

Combined Bleaching Technique: Efficacy and Tooth Sensitivity

The aim of this clinical study is to evaluate the efficacy and dental sensitivity associated with Combined Bleaching Technique (in-office + at-home) varying in-office bleaching application under two different time protocols, and dentifrice containing arginine 8% and carbonate calcium use. One hundred eight participants who meet the study inclusion criteria will be selected. The desensitizing agent used will be a dentifrice containing 8% arginine and calcium carbonate. In each evaluation will be determined: tooth sensitivity and color. The data collected will be submitted to the factorial statistical analysis for evaluation of color and chi-square test for tooth sensitivity (α = 5%).

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Key information

Conditions

Tooth Bleaching Dentin Sensitivity Stomatognathic Diseases Tooth Diseases Tooth Sensitivity

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

About this study

This study will be conducted under the CONSORT recommendations. After approval by the Ethics Committee for Research duly registered, the trial will be conducted in the clinic of dental school at the Federal University of Goias located in Goiania. One hundred eight participants 108 volunteers will be selected on the criteria that qualify inclusion and exclusion from the study will be reported all volunteers were examined not qualify under the criteria for inclusion as part of the initial according to CONSORT recommendations .

After signing the signed an informed consent form all volunteer participants will receive a dental prophylaxis with pumice and water in a rubber cups for the removal of extrinsic stains two weeks before the beginning of tooth whitening.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Upper and lower anterior teeth without restorations;
  • Upper and lower anterior teeth that have never undergone a bleaching procedure and are A2 or darker in color compared to the Vita Classical).

Exclusion criteria

  • Presence of primary and/or secondary carious lesion (s) on upper and lower anterior teeth;
  • Presence of non-carious lesions, such as abfraction, erosion and abrasion;
  • Presence of clinically visible cracks or defects of dental enamel on the dental surfaces of the upper and lower anterior teeth;
  • Use of fixed orthodontic appliances;
  • Presence of tooth sensitivity classified as equal to or greater than mild;
  • Presence of severe dental dimming;
  • Presence of parafunctional habits;
  • Presence of any oral pathology;
  • Smokers;
  • pregnant and lactating women

Treatment and study plan

Combined Bleaching(2x20)

Procedure

one clinical session with two applications of 35% hydrogen peroxide of 20 minutes each. 10% carbamide peroxide for two hours daily over the course of two weeks.

Combined Bleaching(2x20) with arginine

Procedure

one clinical session with two applications of 35% hydrogen peroxide of 20 minutes each. 10% carbamide peroxide for two hours daily over the course of two weeks.

Combined Bleaching (1x20)

Procedure

one clinical session with one application of 35% hydrogen peroxide of 20 minutes each. 10% carbamide peroxide for two hours daily over the course of two weeks.

Combined Bleaching(1x20) with arginine

Procedure

one clinical session with one application of 35% hydrogen peroxide of 20 minutes each. 10% carbamide peroxide for two hours daily over the course of two weeks.

8% arginine and calcium carbonate

Drug

using during all the treatment.

Other names: dentifrice containing carbonate arginine

Primary outcomes

  1. Tooth Sensitivity (TS)

    Time frame: during bleaching, and up to 48 hours postbleaching

    Tooth sensitivity (TS) was evaluated using a five-point rating scale (NRS), in which 0 = none (minimum value), 1 = mild, 2 = moderate, 3 = considerable, and 4 = severe (maximum value); and a visual analogue scale (VAS) in wich each participant placed a line perpendicular to a 10-cm-long line (on which 0 referred to "no pain" (minimum value) and 10 referred to "severe pain" (maximum value)).

    Tooth sensitivity (TS) was evaluated during bleaching, and up to 48 hours postbleaching. The worst TS score or numeric value obtained in each assessment was considered for statistical purposes. It was calculated an average to obtain the median.

Secondary outcomes

  1. Color Evaluation

    Time frame: The evaluations were performed in the baseline period and one month after the treatment

    Objective color evaluation:

    The shade was determined using spectrophotometer VITA Easyshade, in which the parameters L*, a*, and b*, in which L* represents the value from 0 (black) to 100 (white) and a* and b* represent the shade, where a* is the measurement along the red-green axis and b* is the measurement along the yellow-blue axis.

    The color alteration (ΔE) was determined by the differences between the values obtained at baseline and one month after the treatment, which was calculated with the formula: ΔE = [(ΔL *) 2 + (Δa *) 2 + (Δb *) 2]1/2.

    In the Outcome Measure Data Table it was presented Mean and Standard Deviation of the color alteration (ΔE) between Baseline vs one month after bleaching for each group.

Sponsors and collaborators

Lead sponsor

Terezinha de Jesus Esteves Barata

Other

Registry information

Official study title

Combined Bleaching Technique: Efficacy and Tooth Sensitivity - A Randomized, Double Blind Clinical Trial

Important dates

Study start
2016
Primary completion
2016
Study completion
2018
First posted
Mar 24, 2017
Registry last updated
Aug 5, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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