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Clinical Trials/NCT06500546
NCT06500546Not yet recruitingNot Applicable

The Effect of Different Adhesion Strategies on the Clinical Success of Non-caries Cervical Restorations.

Istanbul University0 sites41 target enrollmentStarted: September 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
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

Other

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

Other

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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mustafa Demirci

Prof.Dr.

Istanbul University

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