Health Trials

The Clinical Performance of Two Dentine Replacement Materials in Deep Occlusal Cavities (Randomized)

ConditionsClass I Cavities in High Caries RiskClass I Composite RestorationsRandomized Clinical TrialOcclusal CariesFiber Reinforced CompositeInjectable CompositeComposite RestorationComposite Resins
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorDalia Sameh Fawzi

About this trial

Higher mechanical properties are needed to restore structurally compromised posterior teeth, short fiber reinforced resin composite and injectable bioactive resin composites provide superior properties to flowable composites that were traditionally used to improve adaptation in deep cavities below the packable resin composite restorations. Thus, this study was designed to assess the clinical outcome of high strength dentine substitute materials.

Eligibility criteria

Qualifiers

Adult patients aged (20-50)

Medically free

Good oral hygiene (Plaque index ≤2 (Moderate accumulation with plaque in the sulcus))

Patients accepting to participate in the study.

Disqualifiers

Patients <20 and >50.

Teeth with proximal lesions.

Patients with bad oral hygiene (Plaque index >2).

Systematic disease that may interfere with the study.

Trial design

Treatments tested in this trial

  • Beautifil Flow Plus X
  • EverX Flow

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Dalia Sameh Fawzi

Lead sponsor

Future University in Egypt

Sponsor institution

Source ClinicalTrials.gov