- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06807125
Wear Measurement of Opposing Enamel to Milled Resin Matrix Ceramic Versus Bulk Fill Resin Composite After 2 Years
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
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Giza, Egypt, 3220001
- Misr University for Science and Technology
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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 |
|---|---|
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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).
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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:
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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:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Amount of Enamel Wear
Time Frame: two years follow up
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amount of enamel wear measured through superimposition of STL files exported from intraoral scanner then using geomagic Control X 3D
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two years follow up
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Collaborators and Investigators
Investigators
- Principal Investigator: Esraa EE Hussien, PhD, Misr University for Science and Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-0063
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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