The Effect of Different Adhesion Strategies on the Clinical Success
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Treatment of cervical lesions.
- Who it may be relevant to
- Registry conditions: Poor Aesthetic of Existing Restoration of Tooth, Dental Restoration Failure of Marginal Integrity, Unacceptable Morphology of Tooth Restoration, Secondary Caries. Basic parameters: 14 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect of Different Adhesion Strategies on the Clinical Success of Non-caries Cervical Restorations.
Overview
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.
Interventions
- Procedure Treatment of cervical lesions
Four non-carious cervical lesions from patients will be separated into four groups according to according to the adhesion trategies described below: 1. adhesive material will be applied in total-etch mode, 2. adhesive material will be applied in self-etch, 3. universal adhesive material will be applied for 10 sec. in total-etch mode, which includes rubbing, 4. universal adhesive material will be applied for 10 sec. in self-etch mode, which includes rubbing,
Primary outcome measures
- retention rate of restorations [Time frame: Restorations will be evaluated 1 week, 6 months, 12 months and 24 months after finishing.]
Secondary outcome measures (1)
- retention rate of restorations [Time frame: Restorations will be evaluated 36 months, 48 months and 60 months after finishing.]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06500546 · 2018/58