Clinical evaluation of Clearfil photoposterior: 3-year results

The purpose of this study was to evaluate a new resin composite/bonding restorative system in clinical trials involving human subjects. Sixty restorations were inserted in Class I and Class II preparations in premolars and molars. The enamel margins of the preparations were etched for 60 seconds with 37% phosphoric acid gel. The dentinal surfaces of cavity preparations were etched for 40 seconds with 37% phosphoric acid in glycerine (K-etchant gel) and bonding agent (Clearfil Photo Bond) applied. A resin composite (Clearfil Photoposterior) was placed in three increments with a 20 second light cure of each increment and a 60 second light cure of the final increment. All the restorations were evaluated using the USPHS system and M-L indirect scale. At 36 month recalls, compared to baseline, surface texture for essentially all the restorations was rated Bravo, while all other characteristics were rated Alpha. Secondary caries was reported for one restoration during the third year of clinical use. Wear showed an adjusted mean value of 14.6 microns at 36 months or 4.9 microns per year. No cases of clinical post-operative sensitivity to hot, cold, percussion and foods were reported during the length of the study. Clearfil Photoposterior resin composite system has exhibited remarkable wear resistance and no post-operative sensitivity throughout the length of the study.