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The study will involve 41 people who regularly seek treatment at clinics. Participants must be in generally good health and be older than eighteen. must have at least 20 teeth in an occlusion and maintain appropriate dental hygiene. They have to be treated for a minimum of four non-cancerous cervical lesions in their mouths.Four non-carious cervical lesions from patients will be separated into four groups, and adhesive material will be applied to the lesions in each group using different procedures. Evaluation will be performed based on World Dental Federation (FDI) criteria after initial, ½, 1, 2, 3, 4, and 5 years.
The study will involve 41 people who regularly seek treatment at clinics. Participants must be in generally good health and be older than eighteen. must have at least 20 teeth in an occlusion and maintain appropriate dental hygiene. They have to be treated for a minimum of four non-cancerous cervical lesions in their mouths.Four non-carious cervical lesions from patients will be separated into four groups, and adhesive material will be applied to the lesions in each group using different procedures. Evaluation will be performed based on World Dental Federation (FDI) criteria after initial, ½, 1, 2, 3, 4, and 5 years. In each evaluation period, esthetic (surface gloss, surface coloration, marginal discoloration, color match and translucency, esthetic anatomic form), functional (fracture and retention, marginal adaptation), and biologic criteria (postoperative sensitivity and vitality, caries recurrence) will be evaluated.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adhesion Strategies | Other | Four non-carious cervical lesions from patients will be separated into four groups according to differnet adhesion strategies |
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| Different procedure | Other | All lesions to which adhesives are applied according to different adhesion strategies will be restored with the same type of composite material. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Treatment of cervical lesions | Procedure | Four non-carious cervical lesions from patients will be separated into four groups according to according to the adhesion trategies described below:
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| Measure | Description | Time Frame |
|---|---|---|
| retention rate of restorations | survival of restorations discoloration, color match, translucency, esthetic anatomic form), functional (fracture and retention, marginal adaptation), and biologic criteria (postoperative sensitivity). and vitality, caries recurrence) | Restorations will be evaluated 1 week, 6 months, 12 months and 24 months after finishing. |
| Measure | Description | Time Frame |
|---|---|---|
| retention rate of restorations | survival of restorations discoloration, color match, translucency, esthetic anatomic form), functional (fracture and retention, marginal adaptation), and biologic criteria (postoperative sensitivity). and vitality, caries recurrence) | Restorations will be evaluated 36 months, 48 months and 60 months after finishing. |
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Inclusion Criteria:
Exclusion Criteria:
under the age of 18
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comparison of restoration success
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