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Evaluation in the level of pain and color change in the Different Application Times of the In-office Bleaching

Evaluation of the efficacy and sensitivity of Applying Different In-office Whitening Times: randomized clinical trial - HP Hydrogen Peroxide

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-86fjm3h
Enrollment
Unknown
Registered
2023-09-19
Start date
2021-09-01
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

Dentin Sensitivity. Esthetics.

Interventions

Co-participatory randomized clinical trial in humans. Eighty-four (84) research subjects - 42 residents in the State of Rio de Janeiro and 42 in the State of Sergipe - with a minimum age of 18 years o
Experimental Group 2 - single application for 40 minutes
Control Group - two applications of the bleaching gel for 20 minutes each, in the same appointment, one after the other. A randomization list will be created by an operator that will not participate i

Sponsors

Universidade Salgado de Oliveira
Lead Sponsor
Centro Universitário Maurício de Nassau
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Any individual presenting interest in tooth bleaching who is at least 18 years old; Patients who have maxillary anterior canines with a color equal to or darker than 2.5 M2 (on the Vita Bleachguide scale); Agree to participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Presence of restorations in the upper anterior teeth. Presence of visible cracks in the upper and lower anterior teeth. Presenting any pre-existing general and/or oral medical condition that puts the individual at risk during the study. Being pregnant or lactating. Dental treatment planned to be performed during the course of the study. Generalized periodontal disease. Complex intrinsic staining due to tetracycline, fluorosis or hypocalcification. Presence of tooth sensitivity, patients who have already undergone bleaching procedures; patients who have a bruxism habit or any other pathology that can cause sensitivity (recession, dentin exposure). Teeth with active or chronic caries lesions in the elements.

Design outcomes

Primary

MeasureTime frame
The application of the bleaching gel for a reduced time (single application of 20 min), will promote less sensitivity than the control group (2 applications of 20 min each), but also less bleaching potential. The data will be evaluated using statistical analysis

Secondary

MeasureTime frame
The application of the bleaching gel for 40 minutes directly, and without exchange, will promote color alteration and sensitivity level similar to the control group (2 applications of 20 minutes each). The data will be evaluated through statistical analysis

Countries

Brazil

Contacts

Public ContactEloah Almeida

Universidade Salgado de Oliveira

eloahnunes@id.uff.br55(21)983217757

Outcome results

None listed

Source: REBEC (via WHO ICTRP)