The effect of different restorative material in the cervical of teeth
Phase 2
- Conditions
- one carious cervical lesions.
- Registration Number
- IRCT2015121925607N1
- Lead Sponsor
- Vice chancellor for research of Esfahan university of medical science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
None carious lesions; depth of lesions 2 mm or more; enamel and dentin involvement without pulpal involvement and mobility of tooth; lesions in buccal surface
Exclusion criteria: Carious lesions; patients with poor oral hyegin; history of bruxism and xerostomia; complicated systemic conditions; sever choronic periodontitis and sever attrition(more than 50% loss of occlusal and incisal )
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Retention. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.
- Secondary Outcome Measures
Name Time Method Marginal integrity. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.;Marginal Discoloration. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.;Recurrent Caries. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.;Surface Texture. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.;Anatomic Form. Timepoint: 6 and 12 Months after intervention. Method of measurement: USPHS Chart.