Health TrialsbyHealthPanel

Hybrid Resin Composite vs. Hybrid Ceramic Onlays for Restoring Carious Molars

ConditionCarious Molars
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorPeter Medhat Youssef Gerges

About this trial

The goal of this clinical trial is to compare the clinical performance of hybrid resin composite and hybrid ceramic onlays in restoring carious molars. It will also evaluate the wear resistance of both materials. The main questions it aims to answer are:

* Does the hybrid resin composite or hybrid ceramic onlay perform better in clinical settings over time? * How much wear occurs in each type of onlay over 18 months?

Researchers will compare SHOFU Ceramage (hybrid resin composite) to SHOFU Block HC Hard(hybrid ceramic) to see which material performs better in restoring molars with extensive caries.

Participants will:

* Receive either a hybrid resin composite or hybrid ceramic onlay for their molar cavities. * Visit the clinic for checkups at baseline, 6 months, 12 months, and 18 months. * Undergo visual assessments of their restorations and quantitative wear analysis during follow-ups.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Able to tolerate necessary restorative procedures

Willing to sign the informed consent

Accepts the follow-up period

Disqualifiers

ICDAS 4/5 cavities in first and second permanent molars

Onlay cavities with at least one cusp coverage

Patients with acceptable oral hygiene

Trial design

Design model

Parallel

Treatments tested in this trial

  • SHOFU Block HC Hard

    Other intervention

    Cementation of hybrid ceramic onlay (SHOFU Block HC Hard) on carious molars.

  • SHOFU Ceramage

    Other intervention

    Cementation of hybrid resin composite onlay (SHOFU Ceramage) on carious molars.

Treatment groups

64 Participants
are divided into 2 treatment groups
Group A: Hybrid Ceramic OnlayActive comparator 1 intervention
Group B: Hybrid Resin Composite OnlayExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Clinical Performance

Measured using modified USPHS criteria

Time frame
From baseline to 18 months

Secondary outcomes

1

Quantitative Wear Analysis

Measured in micrometers (μm) using a three-dimensional surface-based superimposition software

Time frame
From baseline to 18 months

Other outcomes

Sponsors and contacts

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

Peter Medhat Youssef Gerges

Lead sponsor

Cairo University

Sponsor institution

Source ClinicalTrials.gov
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