Bulk-Fill Composite Restorations: Clinical Evaluation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAtaturk University

About this trial

This randomized controlled clinical study aims to evaluate the clinical performance of five different bulk-fill composite materials representing distinct technological approaches according to the World Dental Federation (FDI) criteria. The materials include a thermoviscous bulk-fill composite applied with preheating, a sonic-activated bulk-fill composite, a flowable bulk-fill composite, an ORMOCER-based bulk-fill composite, and a conventional bulk-fill composite. Restorations will be clinically assessed at baseline, 1 month, 6 months, and 12 months for esthetic, functional, and biological outcomes.

Eligibility criteria

Qualifiers

Patients aged 18 years and older

Patients in good general health (systemically healthy)

Patients with good oral hygiene

Patients with good periodontal health

Disqualifiers

Presence of any systemic disease

Poor oral hygiene

Presence of active or severe periodontal disease

Teeth with previous restorations or endodontic treatment

Trial design

Treatments tested in this trial

  • Thermoviscous bulk-fill composite restoration
  • Sonic-activated bulk-fill composite restoration
  • Flowable bulk-fill composite restoration
  • ORMOCER-based bulk-fill composite restoration
  • Conventional bulk-fill composite restoration

Treatment groups

70 Participants
are divided into 5 treatment groups

Sponsors and collaborators

Ataturk University

Lead sponsor

Atatürk University Scientific Research Projects Coordination Unit

Collaborator