# Non-syndromic Inherited Anomalies of Mineralized Tooth Tissues: a Whole Exome Study to Identify New Pathogenic Variants

> **NCT03810859** · NA · UNKNOWN · sponsor: **Assistance Publique - Hôpitaux de Paris** · enrollment: 14 (actual)

## Conditions studied

- Amelogenesis Imperfecta
- Dentinogenesis Imperfecta
- Dentin Anomalies

## Interventions

- **BIOLOGICAL:** Blood sample

## Key facts

- **NCT ID:** NCT03810859
- **Lead sponsor:** Assistance Publique - Hôpitaux de Paris
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-10-09
- **Primary completion:** 2022-09-15
- **Final completion:** 2022-09-15
- **Target enrollment:** 14 (ACTUAL)
- **Last updated:** 2021-11-22

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03810859

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03810859, "Non-syndromic Inherited Anomalies of Mineralized Tooth Tissues: a Whole Exome Study to Identify New Pathogenic Variants". Retrieved via AI Analytics 2026-07-26 from https://api.ai-analytics.org/clinical/NCT03810859. Licensed CC0.

---

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