- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06600360
Accuracy of Teledentistry for Diagnosis and Treatment Need in Dental Caries Detection Versus Clinical Examination on a Group of Egyptian Children: A Diagnostic Accuracy Study
February 26, 2025 updated by: Pancee Adel Abdel Aziz Wafi, Cairo University
The aim of this study is to assess the accuracy of teledentistry for diagnosis and treatment need in dental caries detection versus clinical examination on a group of Egyptian children.
Study Overview
Detailed Description
The objective of this study is to assess the precision of using the mobile photographic method of teledentistry for dental caries diagnosis and treatment need of pediatric Egyptian children.
This will be assessed by measuring the diagnostic accuracy of the mobile photographic method versus direct clinical oral examination for the same group of participants.
Study Type
Observational
Enrollment (Estimated)
102
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Pancee A Wafi, BSc
- Phone Number: 002 +20 01006150228
- Email: pancee.adel@dentistry.cu.edu.eg
Study Contact Backup
- Name: Perihan A Wafi, BSc
- Phone Number: 002 +20 01006150247
- Email: perihan.adel@dentistry.cu.edu.eg
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
- Child
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Participants are Egyptian children with dental caries attending the diagnostic center at the Pediatric Dentistry and Dental Public Health Department, Faculty of Dentistry, Cairo University, Egypt.
Description
Inclusion Criteria:
- Egyptian pediatric patients aged 4 to 12 years with a chief complaint of dental caries with or without pain.
- Both genders are included.
Exclusion Criteria:
- Egyptian pediatric patients with systemic conditions that will affect their treatment needs.
- Refusal of participation.
- Refusal to sign the informed consent.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Teledentistry for dental caries detection
Time Frame: 3 months
|
By measuring the accuracy of mobile photographic method of teledentistry for dental caries detection
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical dental caries examination
Time Frame: 3 months
|
By measuring the accuracy of clinical dental caries examination
|
3 months
|
|
Reliability of treatment needs
Time Frame: 3 months
|
By measuring the accuracy of teledentistry for treatment need
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
May 1, 2025
Primary Completion (Estimated)
September 15, 2025
Study Completion (Estimated)
October 15, 2025
Study Registration Dates
First Submitted
September 13, 2024
First Submitted That Met QC Criteria
September 13, 2024
First Posted (Actual)
September 19, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 26, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TELE24
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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