The Effect of Different Adhesion Strategies on the Clinical Success

Istanbul University

Status: Not yet enrolling

Conditions: Poor Aesthetic of Existing Restoration of Tooth; Secondary Caries; Unacceptable Morphology of Tooth Restoration; Dental Restoration Failure of Marginal Integrity

Treatments: Procedure: Treatment of cervical lesions

Study type: Interventional

Funder types: Other

Identifiers

NCT06500546

2018/58

Details and patient eligibility

About

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.

Full 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.

Enrollment: 41 estimated patients

Sex: All

Ages: 14 to 75 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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41 participants in 2 patient groups

Adhesion Strategies

Other group

Description:

Four non-carious cervical lesions from patients will be separated into four groups according to differnet adhesion strategies

Treatment:

Procedure: Treatment of cervical lesions

Different procedure

Other group

Description:

All lesions to which adhesives are applied according to different adhesion strategies will be restored with the same type of composite material.

Treatment:

Procedure: Treatment of cervical lesions