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Diagnostic Accuracy of Oral Images, OPGs, Biomarkers and Questionnaires vs. Clinical Assessment for Periodontal Disease (PostNCT07164573)

Diagnostic Accuracy of Oral Images, Orthopantomographs (OPGs), Biomarkers and Self-Reported Questionnaires vs. Clinical Assessment for Detecting Periodontal Health and Disease: a Multi-center Diagnostic Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07406867
Enrollment
2000
Registered
2026-02-12
Start date
2026-03-01
Completion date
2029-03-01
Last updated
2026-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gingivitis, Periodontal Disease, Periodontitis

Keywords

Diagnosis, ArtiLcial Intelligence, Periodontal Diseases, Radiography, Machine Learning, Photography

Brief summary

This multi-center, cross-sectional diagnostic trial evaluates the accuracy of multiple non-invasive screening tools-including self-reported questionnaires, intra-oral photographs, orthopantomographs (OPGs), intraoral scans (IOS), and salivary/microbial biomarkers-for detecting periodontal health and diseases (gingivitis and periodontitis Stages I-IV), using full-mouth clinical periodontal examination as the reference standard. A total of 2,000 participants will be recruited across five international centers. Diagnostic performance (sensitivity, specificity, AUROC) of individual and combined methods will be assessed using logistic regression and machine learning algorithms to establish an optimized multi-modal screening algorithm.

Detailed description

This study is an extension of NCT07164573, with the addition of salivary and microbial biomarker analysis as index tests. While NCT07164573 focuses on questionnaires, oral images, and OPGs, this study incorporates biomarker-based classifiers to evaluate a comprehensive multi-modal diagnostic approach for periodontal disease detection.This is a multi-center, cross-sectional diagnostic accuracy study. The study aims to validate and compare the performance of multiple index tests against a clinical reference standard for the detection of periodontal health and disease. The reference standard for periodontal diagnosis will be a comprehensive full-mouth periodontal examination conducted by trained and calibrated examiners at five international clinical centers. Diagnoses (periodontal health, gingivitis, periodontitis Stages I-IV) will be assigned based on the integration of clinical, radiographic, and demographic data according to the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. The decision-making algorithms proposed by Tonetti and Sanz (2019) will be applied. The index tests under investigation include: 1. A set of self-reported questionnaires, including a modified CDC-AAP questionnaire, OHIP-14, and a dietary survey. 2. Intra-oral clinical photographs captured with a professional camera and a smartphone. 3. A self-performed intra-oral photograph ("selfie"), with and without cheek retractors. 4. Digital orthopantomographs (OPGs). 5. Intraoral scans (IOS). 6. Biomarker analysis of specific proteins and microbial signatures obtained from unstimulated saliva, oral rinse, and subgingival plaque (collected at the Shanghai center only). Data from the index tests will be analyzed using previously developed and validated machine learning models (e.g., HC-Net+ for OPG analysis, a deep learning model for single frontal-view images, and biomarker-based classifiers for periodontal disease detection). The data collected in this study will also be used to further refine these models, particularly to improve the differentiation between gingivitis/Stage I periodontitis and health/Stage II-IV periodontitis. The primary analytical method will involve assessing the diagnostic accuracy of each index test, both individually and in combination, by calculating sensitivity, specificity, and the area under the receiver operating characteristic curve (AUROC) against the clinical reference standard. Logistic regression and machine learning algorithms will be employed to identify the most predictive variables and optimal diagnostic sequences. A total of 2,000 participants will be recruited across the five centers. The study will be conducted in compliance with the Declaration of Helsinki, ICH-GCP guidelines, and relevant STARD and AI-specific reporting guidelines.

Interventions

None listed

Sponsors

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead SponsorOTHER
University of Chieti
CollaboratorOTHER
King's College London
CollaboratorOTHER
University of Roma La Sapienza
CollaboratorOTHER
University of Turin, Italy
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult patients aged 18 years or older. * Seeking dental care at one of the participating study centers. * Ability to understand and willingness to provide written informed consent.

Exclusion criteria

* Edentulous patients (complete tooth loss). * Pregnancy or lactation. * History of periodontal therapy (other than supragingival prophylaxis/cleaning) within the past 12 months. * Use of antibiotic medication within the 3 months prior to enrollment.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracy for detecting periodontitis (Stage II-IV) as determined by the Area Under the Receiver Operating Characteristic Curve (AUROC) of each index test against the clinical reference standardCross-sectional (assessed at the day 1 of participant enrollment)1. Diagnostic accuracy of the AI-based analysis of OPGs (HC-Net+) for detecting periodontitis (Stage II-IV) 2. Diagnostic accuracy of the AI-based analysis of intra-oral photographs for detecting periodontitis (Stage II-IV) 3. Diagnostic accuracy of the self-reported questionnaire (modified CDC-AAP) for detecting periodontitis (Stage II-IV) 4. Diagnostic accuracy of salivary biomarker-based classifiers (specific proteins obtained from unstimulated saliva and oral rinse) for detecting periodontitis (Stage II-IV) 5. Diagnostic accuracy of microbial biomarker-based classifiers (microbial signatures obtained from subgingival plaque) for detecting periodontitis (Stage II-IV) 6. Diagnostic accuracy of combined multi-modal algorithm integrating questionnaires, oral images, OPGs, and biomarkers for detecting periodontitis (Stage II-IV)

Countries

China, Italy, United Kingdom

Contacts

CONTACTMaurizio S. Tonetti
tonetti@hku.hk15000102368

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 1, 2026