- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07775365
AI-Based Prediction of Root Coverage Outcome From Intraoral Photographs
Development and Internal Validation of a Deep Learning Model Predicting the Outcome of Root Coverage Surgery From Preoperative Intraoral Photographs: A Prospective Observational Cohort Study
Przegląd badań
Status
Warunki
Szczegółowy opis
Whether an exposed root surface can be completely covered is the central question in planning mucogingival surgery. The Cairo classification is the current diagnostic standard for that judgement, but assignment of the recession type varies between examiners and prediction of the individual surgical outcome remains largely subjective. In this cohort, consecutive systemically healthy adults with Cairo RT1,RT2 or RT3 gingival recessions are treated by a single operator with a coronally advanced flap combined with a subepithelial connective tissue graft. Recession depth, keratinised tissue width and gingival thickness are recorded at baseline and at three and six months.
Standardised intraoral photographs are obtained at each time point under fixed conditions. A deep learning model is developed to predict the six-month outcome from the preoperative photograph together with baseline clinical variables. Model performance is assessed by discrimination, calibration and prediction error, using the clinical measurement at six months as the reference standard. A secondary analysis examines whether the recession type assigned automatically from the photograph agrees with the type assigned by the examining periodontist. The model is developed and validated internally within this cohort; no external validation set is available. Its output is not shown to the operator and does not influence treatment. Reporting follows the TRIPOD recommendations for prediction model studies.
Typ studiów
Zapisy (Szacowany)
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Muhammed F Dogan, Resident
- Numer telefonu: +905433890065
- E-mail: mfurkandogaan@gmail.com
Lokalizacje studiów
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Istanbul
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Istanbul, Istanbul, Turcja (Türkiye), 34854
- Rekrutacyjny
- Marmara University Faculty of Dentistry Department of Periodontology
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Kontakt:
- Muhammed F Dogan, Resident
- Numer telefonu: +905433890065
- E-mail: mfurkandogaan@gmail.com
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Metoda próbkowania
Badana populacja
Opis
Inclusion Criteria:
- Systemically healthy patients (ASA I or II status) with no contraindications for periodontal surgery.
- Adult patients aged 18 to 65 years.
- Presence of isolated or multiple gingival recessions classified as Cairo RT1, RT2 or RT3 in the maxilla or mandible.
- Patients with good oral hygiene standards, defined as a Full Mouth Plaque Score (FMPS) and Full Mouth Bleeding Score (FMBS) of < 20% at baseline.
- Presence of an identifiable Cemento-Enamel Junction (CEJ) (Crucial for AI segmentation).
Exclusion Criteria:
- Patients with uncontrolled diabetes, immune system disorders, or pregnant/lactating women.
- Teeth with cervical restorations or abrasions that obscure the CEJ.
- Malpositioned or rotated teeth that would distort the photographic angle for AI analysis.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
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Root coverage surgery cohort
Systemically healthy adults aged 18 to 65 years with Cairo RT1,RT2 pr RT3 gingival recessions, treated with a coronally advanced flap combined with a subepithelial connective tissue graft by a single operator and followed for six months.
All participants received the same surgical technique; no comparison group was formed and no participant was assigned to a treatment for the purposes of this study.
Standardised intraoral photographs and clinical measurements were obtained before surgery and at three and six months.
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A coronally advanced flap is raised over the recession defect and a subepithelial connective tissue graft harvested from the palate is positioned beneath it, after which the flap is sutured coronal to the cemento-enamel junction.
Graft thickness, length and width are recorded for each treated site.
The procedure was performed as routine clinical care and was not assigned for research purposes.
Preoperative intraoral photographs and baseline clinical variables are analysed by a deep learning model that predicts the outcome of root coverage surgery.
The model output is not used in clinical decision making and does not influence treatment; it is compared retrospectively with the outcome measured by the treating periodontist at six months.
The same photographs are also used to assign the recession type automatically, which is compared with the clinical assignment.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Accuracy of the model in predicting root coverage at six months
Ramy czasowe: 6 months
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Difference between the root coverage predicted by a model based on preoperative intraoral photographs and baseline clinical characteristics, and the root coverage observed at six months.
Root coverage is expressed as the percentage of the baseline recession depth that is covered, calculated as [(baseline recession depth - six-month recession depth) / baseline recession depth] × 100, from probing measurements made by the treating periodontist from the cemento-enamel junction to the gingival margin.
Predictive accuracy is summarised as the mean absolute error in percentage points across all treated sites.
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6 months
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Sensitivity and specificity of the model at the selected decision threshold
Ramy czasowe: 6 months
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Proportion of sites correctly identified by the model among those that achieved the outcome (sensitivity) and among those that did not (specificity), evaluated at the operating point selected on the receiver operating characteristic curve.
Both proportions are reported with 95% confidence intervals.
The reference standard is the clinical measurement made at six months by the treating periodontist, using a periodontal probe from the cemento-enamel junction to the gingival margin.
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6 months
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Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Calibration of the model
Ramy czasowe: 6 months
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Agreement between the probability predicted by the model and the frequency observed in the cohort, assessed by the calibration slope and intercept and displayed as a calibration plot.
Discrimination indicates whether the model ranks sites correctly; calibration indicates whether the predicted probabilities are numerically correct, and the two are reported separately because a model may rank well while producing miscalibrated probabilities.
The reference standard is the clinical measurement made at six months.
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6 months
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Agreement between the model-assigned and the clinician-assigned recession type
Ramy czasowe: Baseline
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Proportion of treated sites at which the recession type assigned by the model from the preoperative photograph matches the type assigned by the examining periodontist, reported together with quadratic weighted kappa.
The reference standard is the clinical assignment recorded at baseline according to the criteria of Cairo et al.
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Baseline
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Leyla Kuru, Professor, Marmara University Faculty of Dentistry Department of Periodontology
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 2025-09-02/2025-58
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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