Artificial Intelligence (AI)-Powered Thermal Imaging for Gingival Inflammation Detection

February 11, 2025 updated by: Zeynep Turgut Çankaya, Gazi University

AI-Assisted Thermal Imaging for Gingival Inflammation Assessment: A Novel Approach

This study investigates a novel approach for detecting gingival inflammation using thermal imaging and artificial intelligence (AI). Thermal imaging is a technique that utilizes heat to generate detailed images, while AI assists in analyzing these images to identify patterns. Unlike traditional methods that require direct contact or visual examination, this approach is non-invasive, eliminating the need for physical interaction with the gingiva or reliance on subjective assessments.

A key aspect of this study is its focus on individuals with mouth breathing, a condition that complicates gingival health monitoring. By utilizing thermal imaging, the study successfully detected and classified gingival inflammation levels (healthy, mild, moderate, or severe) based on heat distribution patterns. Additionally, specific temperature thresholds were established to differentiate between healthy and inflamed gingival tissues in this patient group, representing a novel contribution to the field.

The developed AI system demonstrated high accuracy in identifying inflammation. This technology has the potential to facilitate earlier detection of gingival disease, even before clinical symptoms become evident. Furthermore, it offers a fast, painless, and reliable method for monitoring gingival health over time, enhancing accessibility and improving patient experience in dental care.

These findings suggest that the integration of thermal imaging and AI could significantly improve the diagnosis and management of gingival diseases. Future research could further refine this technology by expanding the sample size and optimizing analytical models to enhance accuracy and widespread applicability.

Study Overview

Detailed Description

Ethical Approval and Participant Selection This study was initiated following approval from the Ethics Committee of Gazi University (Meeting No: 13, dated 30.07.2024). Participants were selected from individuals presenting to the Department of Periodontology, Faculty of Dentistry, Gazi University.

Determination of Mouth Breathing

The diagnosis of mouth breathing was based on patients' medical history and clinical examination. Participants were asked about the use of oral breathing devices, whether they slept with their mouth open, and whether they experienced nocturnal awakening due to dry mouth. The following diagnostic tests were employed during the clinical examination to confirm mouth breathing:

Participants were instructed to close their lips and breathe through one nostril while the other nostril was occluded. Individuals with nasal breathing exhibited effective alar muscle function, which is typically absent in mouth breathers.

While participants were instructed to breathe normally, a mirror was held horizontally beneath the nostrils bilaterally. The presence of fog on the lower side of the mirror was considered an indicator of mouth breathing.

After evaluating the criteria for mouth breathing, individuals meeting the criteria were enrolled in the study based on the following inclusion and exclusion parameters:

Inclusion Criteria:

Presence of at least 20 teeth Age between 18 and 25 years, with systemic health No history of periodontal treatment within the last six months

Exclusion Criteria:

Presence of any acute infection Use of systemic antibiotics or anti-inflammatory drugs within the past three months History of systemic diseases Pregnancy and/or lactation Presence of xerostomia or drug-induced gingival inflammation Current or former smoking history Acquisition of Thermal Images The thermal camera lens was fixed and focused on the gingival region being imaged throughout the recording process (Optris GmbH, PI 450, Berlin, Germany) [5].

After the initial thermographic image, participants were instructed to rinse with 20°C ice water for 60 seconds. Following the rinse, thermal images were captured at 1, 2, and 3 minutes.

Labeling Process A total of 82 thermal images from 20 participants were resized to 640 × 480 pixels and annotated using an online licensed browser tool (Make Sense AI). A total of 867 labeled data points were generated and divided into a training set (80% of the total) and a testing set (20% of the total) .

The labeling process involved tracing from the midpoint of the interdental papilla tip, following the juxta-gingival level to the midpoint of the adjacent interdental papilla, and extending vertically to the mucogingival junction. From this vertical endpoint, the boundary was traced back parallel to the starting point, returning to the projection of the initial papilla's midpoint. The boundaries were closed vertically at this projection .

Assessment of Inflammation

The degree of inflammation was evaluated using the Gingival Index . Images were categorized into four groups based on the highest inflammation grade observed in the region:

Inflammation 0: Normal gingiva Inflammation 1: Mild inflammation Inflammation 2: Moderate inflammation Inflammation 3: Severe inflammation

Study Type

Observational

Enrollment (Actual)

20

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

    • Çankaya
      • Ankara, Çankaya, Turkey, 06510
        • Gazi University Faculty of Dentistry Department of Periodontology

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

Sampling Method

Non-Probability Sample

Study Population

The participants were selected from individuals presenting to the Department of Periodontology, Faculty of Dentistry, Gazi University who suffers from mouth breathing.

Description

Inclusion Criteria:

  1. Having at least 20 teeth
  2. Being between 18 and 25 years old and systemically healthy.
  3. No periodontal treatment within the last 6 months.

Exclusion Criteria:

  1. Presence of any acute infection
  2. Use of systemic antibiotics or anti-inflammatory drugs within the past three months
  3. History of systemic diseases
  4. Pregnancy and/or lactation
  5. Xerostomia or drug-induced gingival inflammation
  6. Current or former smokers

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
Inflammation 0, Inflammation 1, Inflammation 2, Inflammation 3
Normal Gingiva Mild Inflammation Moderate Inflammation Severe Inflammation
The degree of inflammation was evaluated using the Gingival Index

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Classification Performance of AI Model in Detecting Gingival Inflammation from Thermal Imaging Data
Time Frame: 6 months
The performance of the AI model in detecting gingival inflammation is assessed using classification metrics derived from thermal imaging data. The model's effectiveness is evaluated based on overall accuracy, precision, sensitivity (recall), specificity, and F1-score. The classification process is performed using the XGBoost algorithm, with a 5-fold cross-validation approach to ensure reliability. The final accuracy and performance metrics are calculated as the mean and standard deviation of cross-validation results.
6 months

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Zeynep Turgut Çankaya, Gazi University

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)

July 30, 2024

Primary Completion (Actual)

January 1, 2025

Study Completion (Actual)

January 2, 2025

Study Registration Dates

First Submitted

February 5, 2025

First Submitted That Met QC Criteria

February 11, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 11, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Upon request

IPD Sharing Time Frame

always

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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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