24-Month clinical evaluation of cervical restorations bonded using radio-opaque universal adhesive compared to conventional universal adhesive in carious cervical lesions: A randomized clinical trial.

The aim of the current study was to evaluate the clinical performance of the novel radio-opaque universal adhesive "Scotchbond™ Universal Adhesive Plus" compared to conventional universal adhesive "Single Bond Universal" over 24 months in cervical carious lesions. Fifty participants with cervical carious lesions were randomly allocated into two groups (n = 25); either Scotchbond™ Universal Plus Adhesive (intervention) or Single Bond™ Universal Adhesive (control). Restorations were assessed at baseline, 12 and 24 months using the modified USPHS criteria.