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The clinical performance of a bioactive composite (alkasite-based), a nanohybrid resin composite and a bulk-fill resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 3 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into three groups: a bioactive composite [Cention Forte Ivoclar Vivadent, Schaan, Liechtenstein], a nanohybrid resin composite [Tetric N-Ceram2 (Ivoclar Vivadent, Schaan, Liechtenstein)] and a bulk-fill resin composite [Tetric N-PowerFill2 (Ivoclar Vivadent, Schaan, Liechtenstein)], All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| bioactive composite | Experimental | Cention Forte Ivoclar Vivadent, Schaan, Liechtenstein |
|
| nanohybrid resin composite | Experimental | Tetric N-Ceram2 (Ivoclar Vivadent, Schaan, Liechtenstein) |
|
| bulk-fill resin composite | Experimental | Tetric N-PowerFill2 (Ivoclar Vivadent, Schaan, Liechtenstein) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| bioactive composite | Device | bioactive composite restoration |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical performances of different restorative systems according to FDI criteria | Two year results according to FDI criteria (scores 1-5, 1-very good, 5-poor/replace) | two years |
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Inclusion Criteria:
Exclusion Criteria:
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| ID | Term |
|---|---|
| D014076 | Tooth Diseases |
| ID | Term |
|---|---|
| D009057 | Stomatognathic Diseases |
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| nanohybrid resin composite |
| Device |
nanohybrid resin composite restoration |
|
| bulk-fill resin composite | Device | bulk-fill resin composite restoration |
|