Color Stability of Two Different Resin Matrix Ceramics

March 11, 2025 updated by: Alshaimaa Ahmed shabaan, Fayoum University

Color Stability of Two Different Resin Matrix Ceramics: Randomized Clinical Trial.

This is in vivo study aimed to evaluate the color stability of the newly introduced resin ceramic matrix (cerasmart )& (vita-enamic ) after a one year

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This is in vivo randomized clinical trial aimed to evaluate the color stability and patient satisfaction of the newly introduced resin ceramic matrix (cerasmart )& (vita-enamic ) in posterior endodontically treated teeth through one year follow-up

Study Type

Interventional

Enrollment (Actual)

102

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

  • Egypt
      • Fayoum, Egypt, 63514
        • Faculty of Dentistry- Fayoum 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

18 years and older (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • diagnose need for restoration in endo treated posterior teeth
  • good general health and oral health
  • occlusal stability

Exclusion Criteria:

  • smoking
  • pregnancy
  • use drugs that affect oral health
  • Para functional 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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Enamic group
patient in this group received a restoration with enamic material
Procedure: enamic
the patient received a crown made of enamic ceramic
Active Comparator: Cerasmart group
patient in this group received a restoration with Cerasmart material
Procedure: cerasmart
the patient received a crown made of cerasmart ceramic

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
color change
Time Frame: 12 months
measurement of restoration using digital spectrophotometer
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
patient satisfaction
Time Frame: 12 months
patient satisfaction is measured self questionnaire to patient consist of 5 questions with 4 answers each answer take a score from 1 to 5 where 1 is the patient is not satisfied at all and 5 is the patient is totally satisfied
12 months

Collaborators and Investigators

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

Sponsor

Fayoum University

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.

General Publications

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)

June 1, 2021

Primary Completion (Actual)

June 1, 2022

Study Completion (Actual)

August 1, 2022

Study Registration Dates

First Submitted

August 12, 2022

First Submitted That Met QC Criteria

August 12, 2022

First Posted (Actual)

August 15, 2022

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 11, 2025

Last Verified

August 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • COST 315

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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