The aim of this randomized clinical trial is to compare the six months clinical performance of the self-adhesive bulk-fill composite with the conventional nano-hybrid composite in the cervical lesions of teeth in the esthetic zone. In addition, to evaluate patient's satisfaction towards the self-adhesive bulk-fill material and its total operatory time.
Cervical lesions.
Cervical lesions of at least one mm depth; to include enamel and dentin.
Cervical lesions of not more than 3 mm in depth.
Male or female genders.
Teeth showing signs of pulpitis or periapical pathosis.
Patients older than 60 years.
Patients younger than 18 years old.
Pregnant women.