Digital Techniques

January 28, 2025 updated by: Eman Hafez Elfky, Faculty of Dental Medicine for Girls

Clinical Performance and Patients Satisfaction of Innovative Digital Techniques for Fabrication of Monolithic Ceramic Crowns

The present study is performed to evaluate clinical performance and patient satisfaction of innovative digital techniques for fabrication of monolithic ceramic crowns

Study Overview

Detailed Description

Digital dentistry has progressed rapidly in the last few years, primarily to improve and enhance the practice of dentistry through the advancement in digital tools and techniques, providing improved accuracy and precision, enhancing patient experience, increasing efficiency and productivity, thereby resulting in better treatment outcomes, whilst also improving clinical outcomes.

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Phase 1

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

      • Cairo, Egypt, 11754
        • Faculty of Dental Medicine for girls Al-Azhar University

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

No

Description

Inclusion Criteria:

  • Patient with posterior molars indicated for full coverage restorations.
  • Patient able to physically and psychologically tolerate conventional restorative procedures.

Exclusion Criteria:

  • Patient in the growth stage with partially erupted teeth.
  • Patient with poor oral hygiene and motivation.
  • Patients with parafunctional habits.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: milled zirconia crowns
this group was received milled zirconia crowns on their posterior molars indicated for full coverage restorations.
-Different digital techniques used for fabrication of the monolithic ceramic crowns were chosen for the current study, Clinical performance of all crowns regarding; marginal adaptation, fracture of restoration during service, color stability and wear behavior will be evaluated according to Modified United States Public Health Service (USPHS) Criteria at base line (1 week), 3 and 6 months after cementation of crowns.
Experimental: milled hybrid ceramic crowns
this group was received milled hybrid ceramic crowns on their posterior molars indicated for full coverage restorations.
-Different digital techniques used for fabrication of the monolithic ceramic crowns were chosen for the current study, Clinical performance of all crowns regarding; marginal adaptation, fracture of restoration during service, color stability and wear behavior will be evaluated according to Modified United States Public Health Service (USPHS) Criteria at base line (1 week), 3 and 6 months after cementation of crowns.
Experimental: 3d printed hybrid ceramic crowns
this group was received 3d printed hybrid ceramic crowns on their posterior molars indicated for full coverage restorations.
-Different digital techniques used for fabrication of the monolithic ceramic crowns were chosen for the current study, Clinical performance of all crowns regarding; marginal adaptation, fracture of restoration during service, color stability and wear behavior will be evaluated according to Modified United States Public Health Service (USPHS) Criteria at base line (1 week), 3 and 6 months after cementation of crowns.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the clinical performance, color stability and wear behavior of monolithic ceramic crowns fabricated using innovative digital techniques.
Time Frame: baseline, 3months and 6 months after crown cementation

Clinical performance of all crowns regarding; marginal adaptation, fracture of restoration during service, color stability and wear behavior will be evaluated according to Modified United States Public Health Service (USPHS) Criteria at base line (1 week), 3 and 6 months after cementation of crowns.

  • Color stability will be evaluated using a spectrophotometer.
  • Wear of restorations will be evaluated using a software analysis.
baseline, 3months and 6 months after crown cementation

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

October 1, 2024

Primary Completion (Estimated)

March 1, 2025

Study Completion (Estimated)

April 1, 2025

Study Registration Dates

First Submitted

January 28, 2025

First Submitted That Met QC Criteria

January 28, 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 28, 2025

Last Verified

September 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • P-CR-23-15

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.

Clinical Trials on Monolithic Ceramic Crowns Fabricated by Different Digital Techniques

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