Bioactive glass to prevent post-operative sensitivity of vital teeth bleaching
- Conditions
- Teeth sensitivityTeeth color changes after bleachingOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
- Registration Number
- ACTRN12621001334897
- Lead Sponsor
- Damascus University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 24
1-be at least 18 years old,
2-Have six maxillary anterior teeth with no restorations or carious lesions on their buccal surfaces,
3-colour shade B2 or darker on the shade guide (Vitapan Classical, Vita
Zahnfabrik)
4-No history of tooth sensitivity or use of a desensitising agent or desensitising toothpaste in the past 3 months.
1-Previous tooth-bleaching procedures,
2-chronic therapeutic drug history,
3-orthodontic appliance use,
4-periodontal disease or active carious lesions,
5-pregnancy or lactation,
6- severe internal tooth discolouration,
7-allergies to bleaching agent or tray material,
8-smoking.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tooth sensitivity using visual analogue scale.[Follow-up will be daily for 7 days after application of both the bleaching agent and the Bioactive/placebo toothpaste. The primary outcome will be assessed by the patients themselves using visual analogue scale in the first day of commencement of intervention.]
- Secondary Outcome Measures
Name Time Method Color changes using digital spectrophotometer.<br>The digital spectrophotometer measures the shade of teeth based on the CIE L*a*b* color space system, allowing the determination of color in a three dimensional space [ Baseline: before the beginning of the intervention. <br>Follow-up will be after 3 days , 1 week ,15 days, 1 month, 3 months and 6 months after intervention commencement of both the bleaching agent and the Bioactive/placebo toothpaste]