Dental Restoration Failure of Marginal Integrity, Poor Aesthetic of Existing Restoration of Tooth, Secondary Caries, Unacceptable Morphology of Tooth Restoration
Conditions
Brief summary
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.
Detailed description
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.
Interventions
PROCEDURETreatment of cervical lesions
Four non-carious cervical lesions from patients will be separated into four groups according to according to the adhesion trategies described below: 1. adhesive material will be applied in total-etch mode, 2. adhesive material will be applied in self-etch, 3. universal adhesive material will be applied for 10 sec. in total-etch mode, which includes rubbing, 4. universal adhesive material will be applied for 10 sec. in self-etch mode, which includes rubbing,
Sponsors
Istanbul University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Intervention model description
comparison of restoration success
Eligibility
Sex/Gender
ALL
Age
14 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Over the age of 18 years * Good oral hygiene normal occlusal relationship with natural dentition * At least 20 teeth are in occlusion The tooth with the lesion must be vital. non-mobile and non-carious * Accepts Healthy Volunteers
Exclusion criteria
under the age of 18 * Poor oral hygiene poor general health condition * Bruxism or uncontrolled parafunction * Patients with periodontal or gingival diseases
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| retention rate of restorations | Restorations will be evaluated 1 week, 6 months, 12 months and 24 months after finishing. | 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) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| retention rate of restorations | Restorations will be evaluated 36 months, 48 months and 60 months after finishing. | 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) |
Outcome results
None listed