About this trial
In this study, a universal adhesive was used with different adhesive techniques (self-etch and total-etch modes) and evaluated for 18 months in three different types of composite material class III and class IV restorations according to the FDI criteria. The hypotheses tested in this study are: (1) clinical success will not differ between different composite materials and (2) clinical outcomes will not differ between different application modes of the universal adhesive.
Eligibility criteria
Qualifiers
Good general health
No heart disease,
No diabetes
No systemic diseases such as hypertension
Disqualifiers
Individuals with advanced periodontitis and associated postoperative sensitivity
Pregnant and breastfeeding women
Individuals undergoing orthodontic treatment and using appliances
Individuals with direct pulp capping
Trial design
Treatments tested in this trial
- Composite materials
Treatment groups
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.