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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03194984
Other study ID # CAAE: 57252216.2.0000.5152
Secondary ID
Status Completed
Phase N/A
First received May 23, 2017
Last updated February 9, 2018
Start date May 15, 2017
Est. completion date January 30, 2018

Study information

Verified date February 2018
Source Federal University of Uberlandia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the effectiveness in terms of color variation, patient satisfaction, absolute risk and intensity of dentin sensitivity due to dental bleaching in the office with 35% hydrogen peroxide (Whiteness HP Automixx 35%, FGM) and Opalescence Boost 38% ( Ultradent, South Jordan, UT, USA) in the same arch in patients of different age groups: 18 to 25 years and 40 to 65 years. Data will be collected, tabulated and submitted to statistical analysis


Description:

Throughout life, the aging of the human being as a whole is inevitable. The dental structure such as cementum and dentin undergo some changes over time, such as secondary deposition of dentin, which results in the reduction of root canal length. In addition, with aging the teeth undergo color changes, presenting a more yellowish or grayish coloration (Ravindra SV et al., 2015). The fact is that most of the studies that involve the technique of dental bleaching have as inclusion factor only young adult patients, excluding patients of more advanced age groups. Therefore, it is fundamental to evaluate the whitening technique in these older patients, since it is a treatment that does not cause harm to the individuals To assess the effect of dental bleaching in the office with Whiteness HP Automixx, FGM at 35% and Opalescence Boost at 38% in the same arch, in different age groups (18 to 25 years and 40 to 65 years) in absolute risk and intensity Of the postoperative dental sensitivity through the visual analog (VAS 0-10) and analogue (NRS 0-4) scales.

- Evaluate the efficacy of Whitening HP Automixx, FGM 35% and Opalescence Boost 38% in the same arch in different age groups (18 to 25 years and 40 to 65 years) using Color Vita Classical and Vita Bleachedguide, and the Vita Easyshade spectrophotometer.

- Evaluate the satisfaction of patients after Whitening HP Automixx at 35, FGM and Opalescence Boost 38% in the same arch in different age groups (18 to 25 years and 40 to 65 years).


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date January 30, 2018
Est. primary completion date January 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients over 18 years of age up to 25 years

- Patients aged 40 years up to 65 years

- Good oral and general health

- Teeth free of restorations or with small restorations

- Free from carious injury,

- Patients with tooth color A2 or darker according to the Vita Classical color scale (Vita Zahnfabrik, Bad Säckingen, Germany)

- Agree to the informed consent form

Exclusion Criteria:

- extensive restoration

- Patients who have already undergone dental whitening

- Pregnant or lactating women

- That report dental sensitivity

- With non-carious cervical lesion

- Parafunctional habits

- Orthodontic appliances

- Any other type of oral pathology

- Smokers, patients who are using analgesic or anti-inflammatory drugs, present systemic alterations such as gastric, cardiac, renal and hepatic problems, diabetics, hypertensives or pre-existing neoplasias.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hydrogen peroxide 35%
The office bleaching products will be applied on one of dental hemi-arch of young patients (18-25 years) or adult patients (40-65 years), after randomization. The product will apllied according manufacture instrutions.
Hydrogen peroxide 38%
The office bleaching products will be applied on one of dental hemi-arch of young patients (18-25 years) or adult patients (40-65 years), after randomization. The product will apllied according manufacture instrutions.

Locations

Country Name City State
Brazil Gisele Rodrigues da Silva Uberlândia Av Pará S/n Bloco 4 L Anexo A Sala 42 Campus Umuarama

Sponsors (3)

Lead Sponsor Collaborator
Federal University of Uberlandia Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Fundação de Amparo à Pesquisa do estado de Minas Gerais

Country where clinical trial is conducted

Brazil, 

References & Publications (4)

de Geus JL, Wambier LM, Kossatz S, Loguercio AD, Reis A. At-home vs In-office Bleaching: A Systematic Review and Meta-analysis. Oper Dent. 2016 Jul-Aug;41(4):341-56. doi: 10.2341/15-287-LIT. Epub 2016 Apr 5. — View Citation

Kossatz S, Dalanhol AP, Cunha T, Loguercio A, Reis A. Effect of light activation on tooth sensitivity after in-office bleaching. Oper Dent. 2011 May-Jun;36(3):251-7. doi: 10.2341/10-289-C. Epub 2011 Jul 8. — View Citation

Martin J, Rivas V, Vildósola P, Moncada L, Oliveira Junior OB, Saad JR, Fernandez E, Moncada G. Personality Style in Patients Looking for Tooth Bleaching and Its Correlation with Treatment Satisfaction. Braz Dent J. 2016 Jan-Feb;27(1):60-5. doi: 10.1590/0103-6440201600127. — View Citation

Reis A, Dalanhol AP, Cunha TS, Kossatz S, Loguercio AD. Assessment of tooth sensitivity using a desensitizer before light-activated bleaching. Oper Dent. 2011 Jan-Feb;36(1):12-7. doi: 10.2341/10-148-CR. Epub 2011 Mar 24. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Tooth discoloration Efficacy of office dental whitening mensured by Easyshade spectrophotometer. 36 weeks
Secondary Dentin sensitivity It will analised the risk and intensity of tooth sensitivity of dental bleaching 36 weeks
Secondary Patient satisfaction It will analised the patient satisfaction by questionnaire of self-perception of aesthetics (PIDAQ) 36 weeks
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