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Recruiting NCT07343063

Evaluation of the Clinical Performance of Different Composite Materials in Class III and IV Restorations.

— Observational Dentin Caries

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: Composite materials.
Who it may be relevant to
Registry conditions: Dentin Caries. Basic parameters: from 18 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
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Evaluation of Anterior Restorations

Overview

In this study, a universal adhesive was used with different adhesive techniques (self-etch and total-etch modes) and evaluated for 18 months in three different types of composite material class III and class IV restorations according to the FDI criteria. The hypotheses tested in this study are: (1) clinical success will not differ between different composite materials and (2) clinical outcomes will not differ between different application modes of the universal adhesive.

Interventions

  • Other Composite materials
    Restorations

Primary outcome measures

  • FDI criteria [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • Good general health
  • No heart disease,
  • No diabetes
  • No systemic diseases such as hypertension

Exclusion criteria

  • Individuals with advanced periodontitis and associated postoperative sensitivity
  • Pregnant and breastfeeding women
  • Individuals undergoing orthodontic treatment and using appliances
  • Individuals with direct pulp capping
  • Individuals with bruxism

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Muhammet Karadaş — Merkez

Identifiers

NCT: NCT07343063 · RTEUDHFMKARADAS006

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗