Accuracy of Artificial Intelligence Technology in Detecting Number of Root Canal of Human Mandibular Second Molar: Diagnostic Accuracy Experimental Study (AI)

December 21, 2025 updated by: Amr Mortada Tony AL-Hadary, Future University in Egypt
to detect the Accuracy of Artificial Intelligence Technology in Detecting Number of Root Canal of Human Mandibular Second Molar: Diagnostic Accuracy Experimental Study.

Study Overview

Study Type

Interventional

Enrollment (Actual)

40

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
        • Future University Dental Hospital

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

-

A- Inclusion criteria:

  1. Patients must be medically free from any systemic disease that can affect root canal treatment.
  2. Age range of the patients should be 18-40 with permanent mandibular second molars indicated for root canal treatment.
  3. No sex predilection.
  4. Patients must have good oral hygiene.
  5. restorable teeth.
  6. Positive patient"s acceptance for participating in the study.
  7. Patients able to sign informed consent.

B- Exclusion criteria:

  1. Lower second molars which are non-restorable, having large perforations, external root resorption, vertical root fracture, internal root resorption, grade 2/3 mobility, previous successful/non-successful root canal treatment
  2. Pregnant women after taking detailed history and pregnancy test must be in the first visit.
  3. Psychologically disturbed patients.

    Teeth that have:

    • Periodontally affected with grade 2 or 3 mobility. 12

    • Not restorable teeth.

    • Abnormal anatomy and calcified canals.

    • Previous root canal treatment.

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: morphology of canals in lower second mandibular molar
Anatomical variations in root canal systems, such as the presence of an additional root canal, are common, and failure to detect all canals can lead to treatment failure.
CBCT scans performed to all participants, will be randomly distributed upon postgraduate students using randomization software
Experimental: Number of canals in lower second mandibular molar
Detection of all canals in patients indicated for root canal therapy in lower second molars by Artificial Intelligence Dental operating microscope and CBCT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of root canals detected
Time Frame: within one year
Detected by AI software
within one year

Collaborators and Investigators

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

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)

November 29, 2024

Primary Completion (Actual)

November 29, 2025

Study Completion (Actual)

December 20, 2025

Study Registration Dates

First Submitted

December 21, 2025

First Submitted That Met QC Criteria

December 21, 2025

First Posted (Actual)

January 6, 2026

Study Record Updates

Last Update Posted (Actual)

January 6, 2026

Last Update Submitted That Met QC Criteria

December 21, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • FUE.REC (46)/11-2024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Time Frame

with in one year

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • ICF

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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