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NCT Number: NCT06500546

The Effect of Different Adhesion Strategies on the Clinical Success

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.

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Key information

Age range

14 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Treatment of cervical lesions

Procedure

Four non-carious cervical lesions from patients will be separated into four groups according to according to the adhesion trategies described below:

  • adhesive material will be applied in total-etch mode,
  • adhesive material will be applied in self-etch,
  • universal adhesive material will be applied for 10 sec. in total-etch mode, which includes rubbing,
  • universal adhesive material will be applied for 10 sec. in self-etch mode, which includes rubbing,

Other names: differnet adhesion procedures

Primary outcomes

  1. 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

  1. retention rate of restorations

    Time frame: 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)

Sponsors and collaborators

Lead sponsor

Istanbul University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2029
First posted
Jul 15, 2024
Registry last updated
Jul 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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