# Genomic Sequencing and Personalized Treatment for Birth Defects in Neonatal Intensive Care Units

> **NCT02551081** · — · RECRUITING · sponsor: **Children's Hospital of Fudan University** · enrollment: 2000 (estimated)

## Conditions studied

- Genetic Disease
- Multiple Malformation
- Congenital Malformation

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT02551081
- **Lead sponsor:** Children's Hospital of Fudan University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2015-10-01
- **Primary completion:** 2025-12-30
- **Final completion:** 2025-12-30
- **Target enrollment:** 2000 (ESTIMATED)
- **Last updated:** 2025-09-05

## Collaborators

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## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02551081

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02551081, "Genomic Sequencing and Personalized Treatment for Birth Defects in Neonatal Intensive Care Units". Retrieved via AI Analytics 2026-07-20 from https://api.ai-analytics.org/clinical/NCT02551081. Licensed CC0.

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