ClinicalTrials.Veeva

Menu

No Code Artificial Intelligence to Detect Radiographic Features Associated With Unsatisfactory Endodontic Treatment

University of Copenhagen logo

University of Copenhagen

Status

Not yet enrolling

Conditions

Apical Periodontitis
Endodontic Underfill
Endodontically Treated Teeth
Endodontic Overfill

Treatments

Device: AI guidance for finding radiographic features

Study type

Interventional

Funder types

Other

Identifiers

NCT06450938
38LZDNHFH5JN

Details and patient eligibility

About

Developing neural network-based models for image analysis can be time-consuming, requiring dataset design and model training. No-code AI platforms allow users to annotate object features without coding. Corrective annotation, a "human-in-the-loop" approach, refines AI segmentations iteratively. Dentistry has seen success with no-code AI for segmenting dental restorations. This study aims to assess radiographic features related to root canal treatment quality using a "human-in-the-loop" approach.

Full description

The emergence of artificial intelligence (AI) and specifically deep learning (DL) have shown great potential in finding radiographic features and treatment planning in the field of cariology and endodontics. A growing body of literature suggests that DL models might assist dental practitioners in detecting radiographic features such as carious lesions, and periapical lesions, as well as predicting the risk of pulp exposure when doing caries excavation therapy. Although, the current literature lacks sufficient research on the interaction of participants and AI in an AI-based platform for detecting features associated with technical quality of endodontic treatment. This prospective randomized controlled trial aims to assess the performance of students when using an AI-based platform for detecting features associated with technical quality of endodontic treatment and predicting the long term prognosis of the treatment. The hypothesis is that participants' performance in the group with access to AI responses is similar to the control group without access to AI responses.

Enrollment

80 estimated patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

1.Being a last year dental student at the university of Copenhagen

Exclusion criteria

  1. Having any previous AI-related experiences
  2. Not accepting to sign the informed consent

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

80 participants in 2 patient groups

participants using guidance from artificial Intelligence
Experimental group
Description:
the experimental arm refers to the group of participants who have access to the AI-based platform for detecting features associated with the technical quality of endodontic treatment. These participants will utilize the AI assistance during the study.
Treatment:
Device: AI guidance for finding radiographic features
Control arm without any guidance from artificial Intelligence
No Intervention group
Description:
the control arm consists of participants who do not have access to the AI-based platform. They will perform the same tasks or assessments as those in the experimental arm but without the assistance of AI.

Trial contacts and locations

0

Loading...

Central trial contact

Shaqayeq Ramezanzade, Phd

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems