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Clinical Study on the effect of Bleaching Toothpastes

Clinical Trial on the effectiveness of Bleaching Toothpastes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7v7tj5
Enrollment
Unknown
Registered
2018-09-17
Start date
2014-08-20
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

Mottled teeth

Interventions

Thirty patients, both genders, over 18 years old, will be randomly assigned to three groups (n = 10), G1: Control - Supervised bleaching with 10% Carbamide Peroxide, G2: Whitening toothpaste 1 and G3:
Procedure/surgery
E06.420.750

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Both genders; older than 18 years; presence of all natural anterior superior teeth; vitalized; naturally or physiologically darkened; without restorations involving the vestibular faces; with color darker or equal to A3 in the VITA scale of the tint guide; good oral health.

Exclusion criteria

Exclusion criteria: Patients with dental sensitivity; cervical lesions or fractures; smokers; pregnant women and infants; children and adolescents (under 18 years of age); previous history of cancerous lesions; caries and periodontal disease; prosthetics and / or previous restorations were excluded.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: To evaluate the effectiveness of tooth whitening with the use of bleaching toothpastes after daily use, according to the manufacturers' instructions for the two groups studied.;The efficacy and speed of the bleaching effect was assessed by color variation (Delta E) after one week of the bleaching session, end of treatment, 15 and 30 days after the end of the treatment, verified by a portable digital spectrophotometer (Easyshade-Vita, Brea, California, USA), according to the CIELab system, based on a variation of at least 5% in pre and post intervention measurements. The evaluated toothpastes were not able to produce a whitening effect similar to supervised bleaching. The durability (maintenance) of the whitening effect obtained with dentifrices is small, with total reversion of the coloration in 30 days.

Secondary

MeasureTime frame
Secondary outcome 1: Evaluate the presence of gingival changes. The incidence of dental sensitivity during and after treatment. The degree of patient satisfaction regarding the result obtained.;Secondary outcome found 1: In each evaluation, the gingival condition was evaluated through clinical examination, where its characteristics were observed as texture and coloration. It was not possible to observe presence of significant gingival alterations for any of the groups. Patients were questioned about the occurrence of dental sensitivity during and immediately after the use of whitening products. The measurement of this sensitivity was done through a visual analog scale, applied through a form filled out by the patient himself. There was no difference between the groups for the reports of sensitivity. At the end of the treatment the patients were evaluated as to the degree of satisfaction with the technique and with the results obtained, by filling out a specific form. The degree of patient satisfaction regarding the result obtained revealed a statistically significant difference between the groups, due to the low whitening effect of the bleaching dentifrices. The obtained data were tabulated and underwent statistical analysis of the descriptive and inferential type.

Countries

Brazil

Contacts

Public ContactKamylla;Renata de Souza e Silva;Guimarães

Universidade Federal de Pernambuco;Universidade Federal de Pernambuco

kamyllayolanda@hotmail.com;renatapguimaraes@gmail.com+55(81)998239606;+55(81)987140518

Outcome results

None listed

Source: REBEC (via WHO ICTRP)