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Tooth Bleaching clinical trials

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NCT ID: NCT03089216 Completed - Tooth Bleaching Clinical Trials

Combined Bleaching Technique: Efficacy and Tooth Sensitivity

Start date: April 1, 2016
Phase: Phase 4
Study type: Interventional

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%).

NCT ID: NCT03039270 Completed - Dentin Sensitivity Clinical Trials

Evaluation of Sensitivity With and Without Sonic Activation of a Desensitizing Gel Before in Office Bleaching in Adults

Start date: January 18, 2016
Phase: N/A
Study type: Interventional

This randomized, controlled clinical trial, triple-blind, split-mouth type was conducted aiming to assess the absolute risk of sensitivity with and without sonic activation of a desensitizing gel previously to the in-office bleaching in adults.

NCT ID: NCT02942082 Completed - Tooth Bleaching Clinical Trials

Clinical Evaluation for Post Bleaching Hypersensitivity Using Desensitizing Agent During In-office Bleaching

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

Evaluating the effect of a desensitizing agent on post-bleaching hypersensitivity.

NCT ID: NCT02841514 Withdrawn - Tooth Bleaching Clinical Trials

The Efficacy and Safety of Tooth Bleaching Procedure Using Y10 Whitening Toothpaste and RF Current

Start date: September 2016
Phase: N/A
Study type: Interventional

Study title: The Efficacy and Safety of tooth bleaching procedure using Y10 Whitening toothpaste and RF current The Device: The Brighttonix Y10 Tooth Whitening system is indicated for use in painless non-invasive tooth whitening treatments. Design: Single center, randomized, controlled, double blind, two-arm, prospective clinical study. Follow up visits at 7 days (phone visit), 12 weeks and 26 weeks.

NCT ID: NCT02463552 Completed - Tooth Bleaching Clinical Trials

Naproxen on Tooth Sensitivity Caused by In-office Bleaching

Start date: May 2015
Phase: N/A
Study type: Interventional

This study aims to evaluate the effects of prior use of non-steroidal anti-inflammatory Naproxen on risk and level of tooth sensitivity caused by in-office bleaching procedures.

NCT ID: NCT02353611 Completed - Tooth Bleaching Clinical Trials

Safety and Efficacy of a 6% Hydrogen Peroxide Tooth Bleaching Agent

Start date: July 2014
Phase: N/A
Study type: Interventional

Bleaching protocol In each session, volunteers received prophylaxis with pumice powder and water. Then, gingival tissue was protected using a light-cured resin gum barrier applied according to the manufacturer's instructions (Lase Protect - DMC, São Carlos, SP, Brazil). Both bleaching agents were prepared by mixing hydrogen peroxide and thickening compounds according to the manufacturer's instructions (with 3 peroxide drops for 1 drop of thickener). The resultant gels were distributed uniformly on the upper hemiarcade surfaces of the teeth. A total of 8 teeth between the first premolars were bleached for each patient. In each bleaching session, the bleaching gels were applied twice for 12 minutes each. In each application, the surface of the gel was light activated with continuous irradiance for 12 minutes using LED/laser light with a total power of 1800 mW (Whitening Lase Plus - DMC Equipamentos, São Carlos, SP, Brazil). Three bleaching sessions were completed for the patients, and the interval between sessions was 7 days