- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06791694
Comparison of Color Measurements of Postgraduate Dental Students Using Different Color Determination Methods (Color)
Comparison of Color Measurements of Postgraduate Dental Students in the Maxillary Anterior Region Using Different Color Determination Methods
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The human eye is effective in detecting subtle differences in tooth color. However, variations in the shade, translucency, opacity, and characterization of a tooth may not be accurately identified. Visual color matching is subject to physiological variables that may lead to inconsistencies, such as age, gender, experience, the type of scale used, varying degrees of light exposure, eye fatigue, and color vision deficiency.
Studies comparing visual and instrumental methods have demonstrated that spectrophotometers yield better results compared to visual color scales. Therefore, it is expected that color measurement devices improve the accuracy of tooth color determination, thereby enhancing the interpretation and aesthetic execution of restorations.
In recent years, the button technique has been described for shade selection in direct aesthetic restorations in the anterior region. In this technique, small composite samples in the form of dots are polymerized on the tooth surface using a curing light. Digital photographs are then taken, and appropriate enamel and dentin shades are selected on a computer using polarized and black-and-white images.
Very few clinical studies have investigated the use of digital color images obtained through intraoral digital scanners for shade selection, comparing them with other existing methods.
The aim of this study is to evaluate the accuracy of shade determination skills in the anterior region by comparing a new technique, the button technique, with other methods and to recommend the most suitable method for shade selection
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Ankara
-
Altındağ, Ankara, Turkey, 06230
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being healthy individuals,
- Not having any systemic diseases,
- Being young individuals (18-40 age range)
- Vital, decay-free and healthy upper central teeth,
- Absence of caries-free hard tissue abrasions, any restoration, fracture, crack, intrinsic or extrinsic discoloration in the upper central teeth
- Lack of removable prosthesis feet for central teeth
Exclusion Criteria:
- Tetracycline, fluorosis staining of upper central teeth
- Patients with dentin exposure or loss of bine in the upper central teeth for any reason
- Pregnant and lactating patients will not be included.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To have compared the inter-observer reliability of 4 different methods used in tooth color selection
Time Frame: 1 month
|
To have compared the inter-observer reliability of 4 different methods used in tooth color selection
|
1 month
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KA-21049
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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