# Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit

> **NCT03831035** · — · COMPLETED · sponsor: **University Hospital, Montpellier** · enrollment: 45 (actual)

## Conditions studied

- Infant, Newborn, Diseases
- Congenital Malformations
- Intensive Care Unit
- Neurologic Symptoms

## Interventions

- **OTHER:** Genetic analyse by whole exome sequencing

## Key facts

- **NCT ID:** NCT03831035
- **Lead sponsor:** University Hospital, Montpellier
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2019-04-08
- **Primary completion:** 2022-06-08
- **Final completion:** 2022-06-08
- **Target enrollment:** 45 (ACTUAL)
- **Last updated:** 2023-11-28


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03831035

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03831035, "Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit". Retrieved via MORVS 2026-10-10 from https://api.morvs.ai/clinical/NCT03831035. Licensed CC0.

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