# Contribution of Optical Genome Mapping (OGM) in the Diagnosis of Multiple Congenital Malformations With or Without Intellectual Disability Without Genetic Abnormality

> **NCT07370792** · NA · RECRUITING · sponsor: **Céline PEBREL-RICHARD** · enrollment: 55 (estimated)

## Conditions studied

- Congenital Malformations

## Interventions

- **GENETIC:** blood sample

## Key facts

- **NCT ID:** NCT07370792
- **Lead sponsor:** Céline PEBREL-RICHARD
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-11-18
- **Primary completion:** 2028-11-01
- **Final completion:** 2028-11-01
- **Target enrollment:** 55 (ESTIMATED)
- **Last updated:** 2026-01-27


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07370792

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07370792, "Contribution of Optical Genome Mapping (OGM) in the Diagnosis of Multiple Congenital Malformations With or Without Intellectual Disability Without Genetic Abnormality". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT07370792. Licensed CC0.

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