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Clinical evaluation and digital monitoring of patients submitted to Home Dental Bleaching

Randomized clinical evaluation and digital Monitoring of patients submitted to Home Dental Bleaching: Effect of wear-time of dental bleaching on the degrees of Collaboration and patient Catisfaction, on the Effectiveness and occurrence of Sensitivity

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-77sbfp
Enrollment
Unknown
Registered
2018-05-04
Start date
2017-08-31
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth Discoloration. Dentin sensitivity.

Interventions

The 66 patients selected will be distributed to each of the 3 study groups. Group I: 22 participants will perform home bleaching with 10% carbamide peroxide gel (Opalescence PF 10%, Ultradent, Utah, U
Sales AgencyGschladt, Hargelsberhg, Austria) included between the two acetate films, 1 mm thick each, at the time of making the trays to be used for the tooth whitening. The trays will be made without
Other
E06.420.750

Sponsors

Faculdade de Odontologia de Araçatuba
Lead Sponsor
Faculdade de Odontologia de Araçatuba
Collaborator

Eligibility

Age
18 Years to 22 Years

Inclusion criteria

Inclusion criteria: Absence of caries injury; Absence of defective or fractured restorations; Absence of periodontal diseases; Good systemic condition; Healthy oral soft tissues; No historical adverse reaction station to peroxides; teeth with a minimum of A2; Absence of dental elements with spontaneous pain; Absence of non-carious cervical lesions and of dentinal tissue exposed in the incisal regions.

Exclusion criteria

Exclusion criteria: Restorations in the vestibular of the central, lateral and canine incisors; Teeth with orthodontic appliances fixed or containing resinous residues after their removal; Pregnant or breastfeeding; Smokers and Patients who routinely use alcohol; Have previously had bleaching treatment; Teeth with fluorosis enamel stains and without pulp; Patients with bruxism habits and those who experienced dental sensitivity prior to the experiment; Did not accept the search consent form; Unavailability of time and commitment to research

Design outcomes

Primary

MeasureTime frame
Expected outcome: Number of patients who have used the trays with the bleaching product according to the recommendations of each study group (2, 4 and 8 hours).

Secondary

MeasureTime frame
Expected outcome: The color change between the initial condition and 14 days after tooth whitening will be analyzed using the Vitapan Classical Shade Guide (Vita Zahnfabrik, Bad Sackingen, Germany) and also with a digital spectrophotometer (Vita Easyshade Advance, Vita Zahnfabrik, Bad Sackingen, Germany).;Expected outcome: The degree of cooperation of the patients, using the tray with the whitening product, will be generated by the TheraMon micro sensor in both dental arches. The interpretation of the results obtained in each of the arcs will be carried out after the completion of the bleaching through the diagram of the time of daily use, in hours, of the trays with the whitening product; considering, therefore, the bleaching time proposed, that is, 2, 4 and 8 hours daily.;Expected outcome: The degree of satisfaction of the patient will be analyzed and measured 14 days after the completion of the bleaching process. To do so, the visual analog method will be used, through a scale of 0 to 10; the patients will be questioned about the degree of satisfaction observed with the dental bleaching performed, being stipulated the value 0 for the patients that did not present any satisfaction and 10 for those who presented the highest degree of satisfaction with the obtained bleaching.;Expected outcome: Dental sensitivity will be analyzed and measured for its presence and intensity 7 days prior to the initiation of the bleaching process, at baseline, after 7, 14 and 21 days after the onset of bleaching, as well as 14 days after the end of whitening. To do so, the visual analog method will be used, through a scale of 0 to 10; the patients will be questioned about the intensity of the discomfort caused by the treatment, being stipulated the value 0 for the patients who did not present any painful symptomatology and 10 when there was a severe sensitivity. 6 In the face of severe sensitivity, the patient will be excluded from the research.

Countries

Brazil

Contacts

Public ContactRenato Sundfeld

Faculdade de Odontologia de Araçatuba

sundfeld@foa.unesp.br+551836363346

Outcome results

None listed

Source: REBEC (via WHO ICTRP)