# Morphology in Oral Rare Syndromes & Artificial Intelligence for Clinical Diagnosis

> **NCT07666269** · NA · NOT_YET_RECRUITING · sponsor: **University Hospital, Bordeaux** · enrollment: 240 (estimated)

## Conditions studied

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

## Interventions

- **OTHER:** intra-oral 3D optical impression

## Key facts

- **NCT ID:** NCT07666269
- **Lead sponsor:** University Hospital, Bordeaux
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-09-01
- **Primary completion:** 2028-03-01
- **Final completion:** 2028-03-01
- **Target enrollment:** 240 (ESTIMATED)
- **Last updated:** 2026-06-24

## Collaborators

- [object Object]
- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07666269

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07666269, "Morphology in Oral Rare Syndromes & Artificial Intelligence for Clinical Diagnosis". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07666269. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*