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Recruiting NCT07343050

Evaluation of the Effect of Flowable Composites on Postoperative Sensitivity in Class I 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: Dental restorations.
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 Dental Restorations

Overview

The aim of this study is to evaluate the effect of flowable conventional and bulk-fill composites on postoperative sensitivity in class I cavities over long-term follow-up. The hypothesis to be tested in this study is that the type of composite material will not affect clinical success.

Interventions

  • Other Dental restorations
    Composite 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

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

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

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

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

Identifiers

NCT: NCT07343050 · RTEUDHFMKARADAS005

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗