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Efficacy of In-office Bleaching with Self-mixed reducing application time: a single-blind randomized clinical trial

Efficacy of in-office Bleaching using 35% Self-mixed Hydrogen Peroxide reducing application time: a single-blind randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-45bk3sw
Enrollment
Unknown
Registered
2024-12-05
Start date
2024-12-15
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

Dentin Sensitivity

Interventions

This randomized, blinded, split-mouth clinical trial aims to clinically evaluate the whitening efficacy in participants undergoing in-office whitening with 35% hydrogen peroxide in the form of a self-

Sponsors

Universidade Estadual de Ponta Grossa
Lead Sponsor
Universidade Estadual de Ponta Grossa
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Volunteers aged at least 18 years; both sexes; with good general and oral health; with teeth free of caries and periodontal disease in the anterior region; who agree to the free and informed consent form (FICF) and whose canines must have A2 color or darker according to the Vita Classical scale (Vita Zahnfabrik, Bad Säckingen, Germany)

Exclusion criteria

Exclusion criteria: Volunteers who have previously undergone a whitening procedure; who have reported the presence of previous dental sensitivity; presence of dental prosthesis; fixed orthodontic appliance; restorations in the upper anterior teeth; endodontic treatment in the upper anterior teeth; gingival recessions; teeth with tetracycline staining or fluorosis; continuous use of medications such as analgesics and anti-inflammatories; pregnant or lactating women and those with habits such as bruxism

Design outcomes

Primary

MeasureTime frame
To evaluate the bleaching efficacy of participants undergoing in-office whitening with 35% hydrogen peroxide in self-mixing with reduced time, assessed by Vita Classical and Bleachedguide Vita shade guide as well as with the Vita Easyshade spectrophotometer.

Secondary

MeasureTime frame
Absolute risk of tooth sensitivity Data collected immediately after the bleaching session, up to 1h after, up to 24h after and up to 48h after the procedure, in each session, using the VAS scale (0-10). Percentage of patients with itooth sensitivity will be called absolute risk of tooth sensitivity;The impact of oral condition on quality of life will be assessed through the Brazilian version of the short form of the Oral Health Impact Profile (OHIP-14), which contains 14 questions, before and after the end of the whitening procedure. Values will be presented as mean and standard deviation.

Countries

Brazil

Contacts

Public ContactAlessandro Loguercio

Universidade Estadual de Ponta Grossa

aloguercio@hotmail.com+55 (42) 3220-3740

Outcome results

None listed

Source: REBEC (via WHO ICTRP)