About this trial
The material under investigation will offer the patient a high strength and high durability restoration with the advantage of having anti-bacterial properties.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Cervical carious lesions in anterior teeth and premolars
Small to moderate class V carious lesion (ICDAS 3 & 4).
Vital upper or lower periodontally sound teeth with no signs of irreversible pulpitis.
Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth
Disqualifiers
Cervical carious lesions in molars.
Deep carious defects (close to pulp, less than 1 mm distance).
Teeth with clinical symptoms of pulpitis such as spontaneous pain or sensitivity to pressure.
Non-vital teeth, Fractured or cracked teeth.
Trial design
Parallel
Treatments tested in this trial
FIT SA
Other interventionself-adhesive flowable giomer restorative material
Beautifil Flow Plus F00
Other interventionConventional flowable giomer restorative material
Treatment groups
Trial outcomes
Primary outcomes
Clinical Performance
Clinical Performance using Modified USPHS criteria
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: