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The Effect of Different Adhesion Strategies on the Clinical Success

Not Applicable
Not yet recruiting
Conditions
Poor Aesthetic of Existing Restoration of Tooth
Secondary Caries
Dental Restoration Failure of Marginal Integrity
Unacceptable Morphology of Tooth Restoration
Interventions
Procedure: Treatment of cervical lesions
Registration Number
NCT06500546
Lead Sponsor
Istanbul University
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.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
41
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Different procedureTreatment of cervical lesionsAll lesions to which adhesives are applied according to different adhesion strategies will be restored with the same type of composite material.
Adhesion StrategiesTreatment of cervical lesionsFour non-carious cervical lesions from patients will be separated into four groups according to differnet adhesion strategies
Primary Outcome Measures
NameTimeMethod
retention rate of restorationsRestorations 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 Outcome Measures
NameTimeMethod
retention rate of restorationsRestorations 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)

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