Health TrialsbyHealthPanel

The Effect of Different Adhesion Strategies on the Clinical Success

ConditionsPoor Aesthetic of Existing Restoration of ToothDental Restoration Failure of Marginal IntegrityUnacceptable Morphology of Tooth RestorationSecondary Caries
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14-75
SponsorIstanbul University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Poor oral hygiene poor general health condition

Bruxism or uncontrolled parafunction

Patients with periodontal or gingival diseases

Trial design

Design model

Parallel

Treatments tested in this trial

  • Treatment of cervical lesions

    Procedure/Surgery

    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,

Treatment groups

41 Participants
are divided into 2 treatment groups
Group A: Adhesion StrategiesOther 1 intervention
Group B: Different procedureOther 1 intervention

Trial outcomes

Primary outcomes

1

retention rate of restorations

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)

Time frame
Restorations will be evaluated 1 week, 6 months, 12 months and 24 months after finishing.

Secondary outcomes

1

retention rate of restorations

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)

Time frame
Restorations will be evaluated 36 months, 48 months and 60 months after finishing.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Istanbul University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: