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Morphology in Oral Rare Syndromes & Artificial Intelligence for Clinical Diagnosis

Geometric Morphometric Characterization of Oro-Dental Anomalies in Rare Bone and Cartilage Diseases From 3D Digital Data (MOSAIC)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07666269
Acronym
MOSAIC
Enrollment
240
Registered
2026-06-24
Start date
2026-09-01
Completion date
2028-03-01
Last updated
2026-06-24

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

Conditions

Artificial Intelligence (AI), Hypophosphatemia, Machine Learning, Mucopolysaccharidoses, Osteogenesis Imperfecta, Palate; Deformity, Rare Bone Disorders, Tooth Abnormalities, X-Linked

Keywords

Rare bone diseases, palatal morphology, geometric morphometrics, 3D intra-oral scan, machine learning, artificial intelligence, diagnostic classification, osteogenesis imperfecta, X-linked hypophosphatemia, mucopolysaccharidosis

Brief summary

MOSAIC aims to determine whether oro-dental morphological anomalies, particularly palatal morphology, associated with rare bone and cartilage diseases can be precisely characterized using 3D digital models analysed through geometric morphometrics. The study will also evaluate whether these morphological signatures can train an artificial intelligence (AI) algorithm to classify syndromes. A prospective monocentric case-control cohort will be constituted, including 3D intra-oral scans and associated clinical data. The final goal is to improve diagnostic accuracy and reduce diagnostic delay in rare bone disorders.

Detailed description

Rare bone and cartilage diseases are genetically heterogeneous conditions in which oro-dental anomalies are frequent yet insufficiently characterized, partly due to subjective clinical assessment and the absence of quantitative tools. Palatal morphology and tooth number/shape anomalies may represent key phenotypic markers but remain underused in diagnosis. Advances in 3D intra-oral scanning and geometric morphometrics now allow precise, reproducible shape analysis of complex anatomical structures. In parallel, artificial intelligence has shown promising results in classifying craniofacial phenotypes from 2D images. However, no study has yet combined 3D digital oral data, geometric morphometrics, and machine learning for rare bone disorders. MOSAIC addresses this gap by building the first structured 3D database dedicated to these conditions and developing a classification model capable of identifying syndrome-specific morphological patterns. Participants will undergo a single visit including an intra-oral 3D optical impression and collection of clinical/genetic data. Geometric morphometric analysis (Generalized Procrustes Analysis, Principal Component Analysis, ProcMANOVA/MANCOVA, Pairwise comparison) will be performed on palatal landmarks configuration. Morphometric outputs will feed supervised machine-learning models (Random Forest, SVM, XGBoost) trained and validated for syndrome classification. Each participant will take part in one single visit (T0) without longitudinal follow-up. Data will then be pseudonymized, processed, and analysed in successive workpackages: (1) database constitution, (2) geometric morphometric analysis, (3) AI model training and validation, (4) internal independent testing. Further external validation is expected through a dedicated follow-up protocol using an independent external dataset. No clinical intervention or therapeutic modification is involved.

Interventions

OTHERintra-oral 3D optical impression

Participants will undergo a single visit including an intra-oral 3D optical impression and collection of clinical/genetic data

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER
UMR 1026 BioTis
CollaboratorUNKNOWN
UMR 5199 PACEA
CollaboratorUNKNOWN
UMR 5259 LAMCOS
CollaboratorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Prospective, observational, monocentric, national case-control study

Eligibility

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

Inclusion criteria

* For cases: Diagnosis of a rare bone and cartilage disorder confirmed by the Rare Disease Competence Center for Constitutional Bone Disorders (MOC) or Calcium and Phosphate Metabolism Disorders (CaP), genetically and/or clinically. * Ability to undergo a 3D intra-oral scan; * Ability of the participant to understand the information notice provided regarding the use of their medical data and 3D digital models for research purposes, and to express informed non-objection to participation in the research. * For controls: healthy adults recruited in the Dental Medicine Department.

Exclusion criteria

* History of major orthodontic/orthognathic treatment; * Craniofacial conditions unrelated to the studied diseases (e.g., cleft palate, non-target craniofacial syndromes); * Impossibility to obtain a 3D optical impression; * Refusal or inability of the participant to understand the information notice and/or to express informed non-objection to participation in the research.

Design outcomes

Primary

MeasureTime frameDescription
Discriminative ability of geometric morphometric analysisat inclusion (Day 0)Discriminative ability of geometric morphometric analysis to differentiate patient subgroups and healthy controls (procMANOVA on Procrustes coordinates, pairwise comparison of Procrustes distance).

Countries

France

Contacts

CONTACTOlivia KEROUREDAN, Dr
olivia.kerouredan@chu-bordeaux.fr05 47 30 43 01
CONTACTAnaïs CAVARE, Dr
05 47 30 43 01

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026