- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07404007
Detection of Proximal Caries in Bitewing Radiography Using Artificial Intelligence
February 4, 2026 updated by: Rawda Hesham Abd ElAziz, Cairo University
Detection of Proximal Caries in Bitewing Radiography Using Artificial Intelligence - A Diagnostic Clinical Study
Using a sequence of bitewing radiographs, Artificial intelligence assists in identifying interproximal caries.
For the identification of dental caries in bitewing, periapical, and panoramic radiographs, a trained deep learning network will be created This study aimed to investigate the reliability of a novel Artificial Intelligence model based on deep learning in the detection of Proximal Caries using Digital Bitewing Radiographs.
(BW).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
2000
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
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Cairo, Egypt, 11331
- Ain Shams University
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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
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Patients attending the Faculty dental out patient clinic who required bitewing radiographic examination for routine diagnosis or treatment planning.
Description
Inclusion Criteria:
- Patients having all Permanent premolars and molars (maximum one tooth missing on each side)
Exclusion Criteria:
- 1-Dental Anomalies →Amelogenesis Imperfecta, Dentinogenesis Imperfecta, taurodontism 2- Severe crowding which prevent visualization of teeth Contacts 3-Orthodontic wires bonded to Enamel of the tooth
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Group 1 Artificial Intelligence Deep learning that is applied in Diagnosis of the proximal Caries
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Artificial intelligence was used as a deep-learning diagnostic tool to detect proximal caries on digital bitewing radiographs.
The system analyzed images and generated probability scores and visual markers for suspected lesions.
Its performance was compared with expert examiner diagnoses as the reference standard.
AI results were used for evaluation only and did not influence patient treatment decisions.
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Group 2 : Digital Bitewing manually annotated by human experts
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Digital bitewing radiographs were manually annotated by calibrated human experts to identify the presence and location of proximal caries.
Annotations were performed using standardized diagnostic criteria and dedicated imaging software to mark suspected lesions.
These expert markings served as the reference standard for comparison with the artificial intelligence outputs.
Inter-examiner agreement was assessed, and disagreements were resolved by consensus.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Reliability of the artificial intelligence model in detecting proximal caries on digital bitewing radiographs
Time Frame: cross-sectional assessment at baseline, with no follow-up period
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cross-sectional assessment at baseline, with no follow-up period
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
January 15, 2023
Primary Completion (Actual)
September 15, 2025
Study Completion (Actual)
December 1, 2025
Study Registration Dates
First Submitted
February 4, 2026
First Submitted That Met QC Criteria
February 4, 2026
First Posted (Actual)
February 11, 2026
Study Record Updates
Last Update Posted (Actual)
February 11, 2026
Last Update Submitted That Met QC Criteria
February 4, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CONS_ Rad 1180
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
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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