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Bleaching efficacy with two protocols in adults

Bleaching efficacy of 35% and 38% hydrogen peroxide with two protocols in adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6g4mj6
Enrollment
Unknown
Registered
2018-07-06
Start date
2016-06-15
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

It is a split-mouth design, double-blind and equivalence randomized clinical trial, to compare two application protocols. The 35% hydrogen peroxide gel Total Blanc Office H35 (Nova DFL, Rio de Janeiro
Other
E06.420.750

Sponsors

Universidade Federal do Amazonas
Lead Sponsor
Universidade Federal do Amazonas
Collaborator

Eligibility

Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: To be included in this study participants had to be aged 18 years or over and had good general and oral health; participants should have at least 6 anterior maxillary sound teeth; at least 1 shade C2 or darker central incisor as assessed by value-oriented shade guide (VITA classical, Vita Lumin, Vita Zahnfabrik, Bad Säckingen, Germany).

Exclusion criteria

Exclusion criteria: Participants with restorations on the labial surface of their anterior teeth and non-carious cervical lesions; with full crowns or veneers; gingival recession; teeth treated endodontically or with spontaneous tooth pain; with internal tooth discoloration; teeth that had fluorosis; pregnant or lactating or had bruxism habits.

Design outcomes

Primary

MeasureTime frame
Color differences between the baseline condition and post-bleaching (1 week and 1 month) will be assessed by Vita Classical and Bleachedguide Vita shade guide as well as with the Vita Easyshade spectrophotometer; data will be presented as means and standard deviations

Secondary

MeasureTime frame
Number of patients that report spontaneous pain in any moment of the bleaching protocol and up to 48 h post-bleaching, through self-report; this number will be presented as percentage of patients with tooth sensitivity and will be named absolute risk of tooth sensitivity;The intensity of tooth sensitivity will be assessed using the visual analogue scale (VAS 0-10) and will be presented as means and standard deviations in different periods (during dental bleaching, up to 1 h, 1 h to 24 h and 24 h to 48 h post-bleaching)

Countries

Brazil

Contacts

Public ContactLuciana Mendonça da Silva Martins

Universidade Federal do Amazonas

luciana.mendonca@gmail.com0055 092 981139290

Outcome results

None listed

Source: REBEC (via WHO ICTRP)