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

NCT ID: NCT06348979

Last Updated: 2024-04-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

110 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2024-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dental Caries

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Hybrid Nano-ceramic (Grandio) CAD/CAM Endocrowns

Adding of short fiber reinforced flowable resin composite material (everX Flow, GC Europe) as a supporting base under CAD/CAM resin composite endocrowns

Group Type EXPERIMENTAL

Fiber flowable (SFRC) support below hybrid nanoceramic endocrowns

Intervention Type PROCEDURE

restoration of endodontically treated teeth by endocrowns

Lithium Disilicate (e.max) Endocrowns

Lithium Disilicate (e.max) Endocrowns

Group Type ACTIVE_COMPARATOR

all ceramic Endocrowns (emax)

Intervention Type PROCEDURE

restoration of endodontically treated teeth by endocrowns

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Fiber flowable (SFRC) support below hybrid nanoceramic endocrowns

restoration of endodontically treated teeth by endocrowns

Intervention Type PROCEDURE

all ceramic Endocrowns (emax)

restoration of endodontically treated teeth by endocrowns

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Grandio CAD/CAM block

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

38 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Sherifa Ahmed Abdelaziz Kandil

Lecturer, Conservative dentistry department, Faculty of Dentistry, Cairo University.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Cairo University

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CEBD 5/2021

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.