About this trial
Most published research on 3D-printed restorative materials is laboratory-based, focusing primarily on mechanical performance and material properties under controlled conditions. While such studies provide important foundational data, they do not fully replicate the complexity of the oral environment. Only a limited number of clinical investigations have directly compared 3D-printed restorations with conventional direct composite restorations in Class II cavities Furthermore, the integration of a digital workflow introduces additional costs and time requirements related to equipment, software, and training. These factors must be justified by demonstrable improvements in clinical outcomes or cost-effectiveness. By evaluating both clinical performance and economic impact, this trial aims to generate practical, real-world evidence that can guide clinicians in selecting appropriate restorative materials and techniques for routine dental practice.
Eligibility criteria
Qualifiers
Adults aged 22 to 45 years.
Low to moderate caries risk.
Normal occlusion.
No signs or symptoms of temporomandibular joint disorders.
Disqualifiers
Bruxism.
Poor cooperation.
Inability or unwillingness to attend follow-up visits.
Anticipated travel during the study period.
Trial design
Treatments tested in this trial
- 3D-printed Ceramic reinforced resin restoration
- bulk fill composite
Treatment groups
Locations
Sponsors and collaborators
Ahmed Reda Abd EL Rahman
Lead sponsor
Cairo University
Sponsor institution