Bulk-Fill Composite Restorations: Clinical Evaluation

ConditionsComposite Resins Dental Caries Class II

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

This trial accepts healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

Thermoviscous bulk-fill composite restoration
Other intervention
Posterior restorations in this group will be performed using a thermoviscous bulk-fill composite material applied after preheating according to the manufacturer's instructions.
Sonic-activated bulk-fill composite restoration
Other intervention
Posterior restorations in this group will be performed using a sonic-activated bulk-fill composite material with reduced viscosity during placement, according to the manufacturer's instructions.
Flowable bulk-fill composite restoration
Other intervention
Posterior restorations in this group will be performed using a flowable bulk-fill composite material according to the manufacturer's instructions.
ORMOCER-based bulk-fill composite restoration
Other intervention
Posterior restorations in this group will be performed using an ORMOCER-based bulk-fill composite material according to the manufacturer's instructions.
Conventional bulk-fill composite restoration
Other intervention
Posterior restorations in this group will be performed using a conventional bulk-fill composite material according to the manufacturer's instructions.

Treatment groups

70 Participants

are divided into 5 treatment groups

Group A: ViscolorExperimental treatment 1 intervention

Group B: SonicFillExperimental treatment 1 intervention

Group C: Estelite Bulk FlowExperimental treatment 1 intervention

Group D: Admira Fusion XtraExperimental treatment 1 intervention

Group E: Filltek Bulkfill CompositeExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Clinical performance according to FDI criteria

The clinical performance of posterior restorations will be evaluated according to World Dental Federation (FDI) criteria, including esthetic, functional, and biological properties.

Time frame

Baseline (1 month), 6 months, and 12 months

Sponsors and contacts

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

Ataturk University

Lead sponsor

Atatürk University Scientific Research Projects Coordination Unit

Collaborator

Source ClinicalTrials.gov

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