Wear Measurement of Opposing Enamel to Milled Resin Matrix Ceramic Versus Bulk Fill Resin Composite After 2 Years

January 29, 2025 updated by: Esraa Esmeail Hussien, Misr University for Science and Technology

Intraoral Wear Measurement of Opposing Enamel to Indirect Milled Resin Matrix Ceramic Versus Direct Bulk Fill Resin Composite in Posterior Teeth After Using 2 Years: Randomized Clinical Trial

This clinical trial conducted to measure the amount of wear of opposing enamel to indirect milled resin matrix ceramic versus direct bulk fill resin composite intraorally using Digital Scanner after two years of using

Study Overview

Status

Completed

Conditions

Detailed Description

Indirect milled resin matrix ceramic overlay versus direct bulk fill resin composite overlay was utilized in a clinical trial to compare the amount of enamel wear on endodontically treated molars using a Panda P2 digital scanner and Geomagic Control X 3D software. After one and two years, measurements of enamel wear were taken.

Study Type

Interventional

Enrollment (Actual)

26

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Giza, Egypt, 3220001
        • Misr University for Science and Technology

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • ● Patients with non vital badly decayed posterior teeth.

    • 18 -55years.
    • Males or Females.
    • Good oral hygiene.
    • Co-operative patients approving to participate in the study

Exclusion Criteria:

  • High caries index.

    • Severe medical complications.
    • Pregnancy.
    • Allergic history concerning methacrylates Disabilities.
    • Heavy smoking.
    • Xerostomia.
    • Lack of compliance.
    • Evidence of parafunctional habits.
    • Temporomandibular joint disorders.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Resin matrix ceramic block
BRILLIANT Crios is the ideal choice for single-tooth restorations, both in the anterior and the posterior region. It is composed of dental glass (barium glass ˂ 1.0 μm), amorphous silica (Sio2 ˂ 20 nm), resin matrix (cross-linked methacrylates) and pigments (inorganic pigments such as ferrous oxide or titanium dioxide).
Milled resin composite block for fabrication of permanent, indirect restorations using a CAD/CAM grinding process. shock absorbing affect due to the dentin- like modulus of elasticity makes BRILLIANT Crios will suited or indirect restoration.
Other Names:
  • CAD/CAM Reinforced composite overlay
Active Comparator: Direct Restoration

3M™ Filtek™ One Bulk Fill Restorative is a visible light activated, restorative composite optimized to create fast and easy restorations. The material can be placed and cured up to 5 mm deep, enabled by a stress relieving resin system and optimized optical properties. It is composed of fillers which are a combination of a non-agglomerated/non-aggregated 20 nm silica filler.

4 to 11 nm zirconia filler, zirconia/silica cluster filler and ytterbium trifluoride filler consisting of 100nm particles. The inorganic filler loading is about 76.5% by weight (58.5% by volume). It contains AFM (dynamic stress-relieving monomer), AUDMA, UDMA and 1, 12-dodecane-DMA. 3M™ Filtek™ Bulk Fill Posterior Restorative is applied to the tooth following use of a methacrylate-based dental adhesive

Milled resin composite block for fabrication of permanent, indirect restorations using a CAD/CAM grinding process. shock absorbing affect due to the dentin- like modulus of elasticity makes BRILLIANT Crios will suited or indirect restoration.
Other Names:
  • CAD/CAM Reinforced composite overlay

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Amount of Enamel Wear
Time Frame: two years follow up
amount of enamel wear measured through superimposition of STL files exported from intraoral scanner then using geomagic Control X 3D
two years follow up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Esraa EE Hussien, PhD, Misr University for Science and Technology

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 10, 2023

Primary Completion (Actual)

January 10, 2024

Study Completion (Actual)

January 10, 2025

Study Registration Dates

First Submitted

January 29, 2025

First Submitted That Met QC Criteria

January 29, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 29, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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