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NCT06348979 Clinical Trial

Clinical Performance of Fiber Reinforced FRC Base and Bonded CAD/CAM Resin Composite Endocrowns

Dental Caries Clinical Trial

Official title:
Clinical Performance of Fiber Reinforced FRC Base and Bonded CAD/CAM Resin Composite Endocrowns Versus Conventional Lithium Disilicate Endocrowns in Posterior Teeth (1y Randomized Clinical Trial)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06348979
Other study ID # CEBD 5/2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date January 30, 2024

Study information
Verified date March 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research proposal is introduced to clinically test short fiber reinforced flowable resin composite material (everX Flow, GC Europe) as a supporting base under CAD/CAM resin composite endocrowns due to gap of knowledge present in this area.

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date January 30, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 38 Years
Eligibility Inclusion Criteria: - Endodontically treated molar teeth indicated for endocrown. - Presence of favorable occlusion and teeth are in normal alignment with the adjacent teeth, -medically free Exclusion Criteria: - ? Endodontically treated molar teeth indicated for post and core or only crown coverage. - Severe periodontal problems

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Fiber flowable (SFRC) support below hybrid nanoceramic endocrowns
restoration of endodontically treated teeth by endocrowns
• all ceramic Endocrowns (emax)
restoration of endodontically treated teeth by endocrowns

Locations
Country Name City State
Egypt Cairo University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary clinical Fracture modified usphs criteria (alpha, bravo, charlie) with measuring unit: scoring system (ordinal) change from baseline and months: 3, 6, 12
Secondary clinical performance marginal adaptation modified usphs criteria (alpha, bravo, charlie) with measuring unit:scoring system (ordinal) change from baseline and months: 3, 6, 12
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