The goal of this clinical trial is to evaluate the clinical performance of Class II restorations of a thermoviscous nanohybrid materials , of a bulk-fill composite resin, and of conventional nanohyribrid bulk-fill composite resins . Class II restorations will be performed in patients using three different restorative materials.And restorations will be evaluated using modified US Public Health Service criteria Resorations will be photograped and restorations will be evaluated for 6,12 months.
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Marginal Adaptation
Timeframe: From baseline to 18 month
Marginal Staining
Timeframe: From baseline to 18 month
Retention
Timeframe: From baseline to 18 month
Seconder caries
Timeframe: From baseline to 18 month
Postoperative sensitivity
Timeframe: From baseline to 18 month