About this trial
The aim of this study is to evaluate the effect of flowable conventional and bulk-fill composites on postoperative sensitivity in class I cavities over long-term follow-up. The hypothesis to be tested in this study is that the type of composite material will not affect clinical success.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
good general health
no heart disease
no diabetes
no systemic diseases such as hypertension
Disqualifiers
Patients with advanced periodontitis and associated postoperative sensitivity,
Pregnant and breastfeeding women,
Patients undergoing orthodontic treatment,
Patients using appliances,
Trial population
The entire study will be conducted at the Restorative Dentistry Department clinic of the Faculty of Dentistry at Recep Tayyip Erdoğan University. Participants who have received routine dental treatment at the university's dental clinic and whose records are kept will be included in the research.
Trial design
Case-control
Prospective
Treatments tested in this trial
Dental restorations
Other interventionComposite restorations
Treatment groups
Trial outcomes
Primary outcomes
FDI criteria
good, very good, poor
Locations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.