Bleaching efficacy with two protocols in adults
- Conditions
- dentin sensitivityC07.793.266
- Registration Number
- RBR-6g4mj6
- Lead Sponsor
- niversidade Federal do Amazonas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
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).
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.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method umber 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)
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