Clinical evaluation of a monochromatic composite resin of dental restoratio
Not Applicable
Recruiting
- Conditions
- Tooth Diseases
- Registration Number
- RBR-8txr4fw
- Lead Sponsor
- niversidade Estadual de Ponta Grossa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Good general health; good oral hygiene; have at least 20 teeth under occlusion. At least two comparable non-carious cervical lesion (in size; shape and dimensions); non-retentive; deeper than 0.5 mm; and involving both enamel and dentin of vital teeth. The cavo-superficial margin cannot involve more than 50% of the enamel
Exclusion Criteria
Extremely poor oral hygiene; using orthodontic devices; severe or chronic periodontitis; heavy bruxism habits. Known allergy to resin-based materials or any other material used in this study. Pregnant or lactating women; chronic use of anti-inflammatory; analgesic and psychotropic drugs
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate color match using a digital spectrophotometer on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed at 6, 12, 24, 36 and 60 months.
- Secondary Outcome Measures
Name Time Method Evaluate the aesthetic properties; functional properties and biological properties using the World Dental Federation (FDI) clinical criteria on the performance of a monochromatic composite versus a traditional composite in non-carious cervical lesions. Interim data analyzes will be performed at 6, 12, 24, 36 and 60 months.