Evaluation of Dental Bleaching In-office

Esthetics, Dental Clinical Trial

— Bleaching  

Official title:

Evaluation of Bleaching In-office With Violet LEd Light (405 nm): Randomized, Controlled Double Blind and Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03192852
• Other study ID #: 2.034.518
• Status: Completed
• Phase: N/A
• Start date: July 1, 2018
• Est. completion date: December 20, 2019

Study information

• Verified date: July 2018
• Source: University of Nove de Julho
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

We aim to evaluate colorimetric changes after supervised whitening treatment, using Violet LED light associated or not with carbamide peroxide 35% gel. 80 will be divided into: Group 1 - Violet LED light, Group 2 Violet LED light + carbamide peroxide 35% gel, Group 3 -hydrogen peroxide 35% and Group 4 will be submitted to the gingivoplasty surgery procedure, for aesthetic desire, after whitening treatment with Violet LED light without gel. The colorimetric changes will be measured before, right after each whitening session in the end of the period of 3 months, through the Vitapan Classical (Vita) color scale, and by digital spectrophotometer. The sensibility degree will be measured by the Visual Analogue Scale (VAS) . The gum tissues Group 4, will be analyzed by histomorphometrically. Quality of life will be evaluated.

Description:

This randomized, blind controlled trial has the objective of evaluate colorimetric changes after supervised whitening treatment, in-office, using Violet LED light of 405 nm associated or not to the use of carbamide peroxide 35% gel. Eighty patients, of which 20 with aesthetics desires to be submitted to gingivoplasty surgery, will be divided into four groups. Group 1 will receive whitening only with Violet LED light (405 nm). Group 2 will receive a whitening treatment combination of Violet LED light with carbamide peroxide 35% gel. Patients of Group 3 will receive a whitening treatment with hydrogen peroxide 35% and Group 4 will be submitted to the gingivoplasty surgery procedure, for aesthetic desire, after whitening treatment with Violet LED light (405 nm) without gel. The colorimetric changes will be measured before, right after each whitening session in the end of the period of 3 months, through the Vitapan Classical (Vita) color scale, and by digital spectrophotometer (SpectroShade™ Micro MHT Optic Research). The sensibility degree will be measured by the Visual Analogue Scale (VAS) in each session and in all groups. The gum tissues removed during the gingivoplasty in Group 4, will be histomorphometric analyzed to measure possible inflammatory gum changes by the Violet LED light (405 nm) irradiation. The degree of satisfaction of the patient and the life quality after aesthetic result achieved will be evaluated. The results will be presented by means and standard deviation. After checking the normality of the data, a one-way ANOVA will be performed. In case the data do not follow a normal distribution, it will be utilized the Kruskal-Wallis test and a value of p <0.05.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: December 20, 2019
• Est. primary completion date: December 20, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• negative medical history,

• Good systemic and oral health

• Patients with aesthetic complaint of discoloration of upper and lower teeth

• Patients with aesthetic desire for gingivoplasty, regardless of color in the baseline (Group 4), without the need for a prosthetic procedure and with sufficient gingiva inserted

• Color in the baseline higher than the A2 of the vita scale for groups 1, 2 and 3.

Exclusion Criteria:

• Patients with dentin hypersensitivity, incisal and occlusal wear or open cavities;

• Patients with pulp alterations;

• Carriers of dental anomalies;

• Patients with dental fractures who do not have restorations on the buccal surface of the teeth to be cleared;

• Patients who have had dental bleaching for less than 2 years;

• Holders of fixed appliances, orthopedic;

• Teeth pigmented by intrinsic factors;

• Smokers;

• Pregnant and Infants;

• Patients reporting adverse reactions to Hydrogen Peroxide;

• Patients who are taking ferrous sulfate medication;

• Patients who use chronic decorticosteroids, as well as volunteers who are taking analgesics or anti-inflammatories.

• Individual or removable prosthesis holders on the analyzed teeth will also be excluded or patients with endodontically treated teeth (Teeth 15-25 and 45-35).

Related Conditions & MeSH terms

• Esthetics, Dental

Intervention

Other:
• dental bleaching
dental bleaching can be achieved with light, light+ peroxide carbamide gel, or only with peroxide carbamide gel

Procedure:
• Gingivoplasty
gengivoplasty will be realized to in illuminated tissue an no illuminated tissue to morphometrically evaluate the tissue

Locations

Country	Name	City	State
Brazil	University of Nove de Julho (UNINOVE)	São Paulo

Sponsors (1)

Lead Sponsor	Collaborator
University of Nove de Julho

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Color Evaluation	Color evaluation will be done before and after each bleaching session through the Vita Classical scale (VITA Zanhnfabrik, BadS?ckingrn, Germany) and SpectroShade ™ Micro MHT Optic Research by a previously trained and blind evaluator in the 4 groups	baseline
Primary	Color Evaluation	Color evaluation will be done 3 months after bleaching through the Vita Classical scale (VITA Zanhnfabrik, BadS?ckingrn, Germany) and SpectroShade ™ Micro MHT Optic Research by a previously trained and blind evaluator in the 4 groups	3 months
Secondary	Pain measured with Visual Analogue Scale (VAS)	The pain will be evaluated through the Visual Analogue Scale (VAS) at each session before and after bleaching in the 4 groups.	baseline
Secondary	Pain measured with Visual Analogue Scale (VAS)	The pain will be assessed through the Visual Analogue Scale (VAS) 3 months after the end of tooth whitening in the 4 groups.	3 months
Secondary	Quality of life measured with Psychosocial Impact Questionnaire	Quality of life will be assessed through the Psychosocial Impact of Dental Aesthetics Questionnaire validated for Brazil at the Federal University of São Paulo (UNIFESP)	baseline
Secondary	Quality of life measured with Psychosocial Impact Questionnaire	Quality of life will be evaluated through the Psychosocial Impact Questionnaire of the Dental Internship validated for Brazil at the Federal University of São Paulo (UNIFESP) 3 months after the end of the bleaching.	3 months
Secondary	Histomorphometric evaluation	will be histomorphometric analyzed to measure possible inflammatory gum changes by the Violet LED light (405 nm) irradiation.	baseline