Clinical study to evaluate the effect of a bioactive restoration material in restoration of dental root caries
Not Applicable
- Conditions
- Cervical dental cariesOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
- Registration Number
- ACTRN12624000653561
- Lead Sponsor
- Damascus University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
patient with minimum age 19
- cervical carious lesions (up to 40% of the lesion on root)
- lesion depth not less than 1 mm
- the lesion must be on:
lower or upper molars
lower or upper premolars
and lower canines only
Exclusion Criteria
- history of tooth hypersensitivity
- periapical or periodontal diseases
- necrotic pulp and endodonticaly treated teeth
- previous restorations
- bruxism
- pregnancy
- sensitivity to any material in the study
- smokers
- using orthodontic appliances
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Retention rate [Rated by modified USPHS criteria<br><br>Alpha: retained<br>Charlie: missing<br> 1 week (Baseline), 3 months post-intervention, 6 months post-intervention, 9 months post-intervention, and 1 year post-intervention (primary timepoint)]
- Secondary Outcome Measures
Name Time Method