The Effect of Different Adhesion Strategies on the Clinical Success of Non-caries Cervical Restorations.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Istanbul University
- Enrollment
- 41
- Primary Endpoint
- retention rate of restorations
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 14 Years to 75 Years (Child, Adult, Older Adult)
- Sex
- All
- Accepts 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
Arms & Interventions
Adhesion Strategies
Four non-carious cervical lesions from patients will be separated into four groups according to differnet adhesion strategies
Intervention: Treatment of cervical lesions (Procedure)
Different procedure
All lesions to which adhesives are applied according to different adhesion strategies will be restored with the same type of composite material.
Intervention: Treatment of cervical lesions (Procedure)
Outcomes
Primary Outcomes
retention rate of restorations
Time Frame: 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 Outcomes
- retention rate of restorations(Restorations will be evaluated 36 months, 48 months and 60 months after finishing.)
Investigators
Mustafa Demirci
Prof.Dr.
Istanbul University
