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Evaluation of whitening and depression on tooth surface after action of whitening toothpastes

Bleaching effect and superficial roughness evaluation of whitening toothpastes during two months follow-up in vivo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4nq793
Enrollment
Unknown
Registered
2020-03-03
Start date
2016-01-01
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

color

Interventions

Toothbrushing 3 times daily according to the groups: Sodium Fluoride (1450ppm), Sodium Fluoride (1100ppm) and Sodium Fluoride (1384ppm). There is no control group.
Procedure/surgery

Sponsors

Universidade Estadual de Campinas
Lead Sponsor
Faculdade Odontologia de Piracicaba da Universidade Estadual de Campinas
Collaborator

Eligibility

Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Volunteers between 18 and 30 years old; independent of gender; with no periodontal disease and caries free; that never bleached their teeth; have no systemic disease and no anterior teeth restoration.

Exclusion criteria

Exclusion criteria: Natural white teeth (B1 or A1 in Vita Classical scale, VITA, Bad Säckingen, SWZ); poor oral hygiene; allergies to any of the products; chronic medicine needs; smoking habits; drugs addiction; caries lesion; extensive posterior restoration and pregnant women.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: there will be a change in the roughness of the dental surface provided through the use of whitening toothpastes after one month of use.;Expected outcome 2: observe that there will be no color change provided by using bleaching toothpastes after one month of use.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactJosué Junior Pierote

Faculdade Odontologia de Piracicaba da Universidade Estadual de Campinas

josuepierote@hotmail.com+55119983060175

Outcome results

None listed

Source: REBEC (via WHO ICTRP)