Impact Of Digital Photography & Conventional Method On The Accuracy Of Dental Shade Matching In The Esthetic Zone

July 26, 2021 updated by: Rawan Ferroukhi, Cairo University

Impact Of Digital Photography & Conventional Method On The Accuracy Of Shade Matching In The Esthetic Zone

The aim of this study:

Is to evaluate the accuracy of digital photography in optimizing shade matching when compared to conventional method of shade selection.

Study Overview

Detailed Description

Randomized control trial, 2 groups will be included. Group 1: Color matching using Vita 3D master, using modified (USPHS) criteria Group 2: Color matching using digital photography using (Photoshop adopt) the assessment will be through a questionnaire for the patient satisfaction outcome using Visual analogue scale

Study Type

Interventional

Enrollment (Actual)

9

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

      • Cairo, Egypt
        • Cairo 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 to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Patients between 18-70 years old, able to read and sign the informed consent document.
  2. Patients requiring restorations in the esthetic zone.
  3. Patients don't have active periodontal or pulpal diseases
  4. Patients willing to return for follow-up examination and evaluation.

Exclusion Criteria:

  1. Patients in the growth stage.
  2. Patients with poor oral hygiene and lack of motivation.
  3. Psychiatric problems or unrealistic expectations.

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: Screening
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: group 1 Color matching using Vita 3D master

Outcome Name: Color Matching measured by :

Modified (USPHS) criteria

Alpha (A)Perfectly matched Beta (B)Not perfectly matched Charlie (C)unacceptable Determent by 10 observers
Other Names:
  • Conventional shade matching
Experimental: group 2 Color matching using digital photography

Outcome Name: Color Matching measured by Digital Photography using (Photoshop)

Software:

  • 0 to 1: no difference in perception
  • 1 to 2: only perceptible to a trained observer
  • 2 to 3.5: perceptible difference
  • 3.5 to 5: marked difference

When taking the image, a gray card is used for subsequent exposure calibration in Adobe Camera Raw (which is packaged with Photoshop).

  • Images are then opened into Photoshop.
  • The "INFO" panel must be open.
  • Click on the small eyedropper in the Info panel window and click on ''Lab Color".
  • Place the mouse over the center of the tooth to be measured for L value.
  • Click on the "HSB Color" option, which stands for hue, saturation, and brightness.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient satisfaction
Time Frame: 1 year
Visual analogue scale
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Color Matching
Time Frame: 1 year
Digital Photography using (Photoshop)/using Vita 3D master Modified (USPHS) criteria
1 year

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Rawan Ferroukhi, Masters in FixedProsthodontics, MSc Student of Fixed Prosthodontics, Division of Fixed Prosthodontics, Faculty of Dentistry, Cairo University, Cairo, Egypt

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.

Helpful Links

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)

July 1, 2018

Primary Completion (Actual)

October 31, 2018

Study Completion (Actual)

August 1, 2019

Study Registration Dates

First Submitted

July 23, 2017

First Submitted That Met QC Criteria

July 23, 2017

First Posted (Actual)

July 25, 2017

Study Record Updates

Last Update Posted (Actual)

July 29, 2021

Last Update Submitted That Met QC Criteria

July 26, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • CEBC-CU-2017-07-17

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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