A clinical study to assess the durability dental restorations made with bioactive restorative materials: a randomized clinical trial

INTERVENTION: E06.323.428 In total, 120 participants with class II carious lesions will be divided into three groups of 40 patients each, restorations will be done according to the manufacturer's instructions of each restorative material used, group TC (control): Tetric N‐Ceram composite resin (Ivoclar Vivadent), EF group: Glass ionomer EQUIA Forte Fill (GC Tokyo, Japan) (experimental group) and CN Group: Alkasite Cention N (Ivoclar Vivadent) material (experimental group). Procedure/surgery CONDITION: C07.793.720.210 dental caries ; K02 ; C07.793.720.210 K00‐K93 PRIMARY OUTCOME: Retention failure of composite restorations will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months The presence of the fracture of the restoration will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months SECONDARY OUTCOME: The presence of the Marginal discoloration of the restoration will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months ; The presence of the recurrence caries will be evaluated by clinical assessment (visual inspection), considering a variation of at least 5% in the measurements after polishing, 6, 12 and 24 months INCLUSION CRITERIA: Patients 12 to 50 years old able to provide valid information; who require at least one class II dental restoration due to active carious lesion or exchange for poor permanent tooth restoration; the tooth selected to receive the restoration must have an antagonist and adjacent tooth; without excessive tooth wear; without evident temporomandibular disorders.