# Perinatal Precision Medicine

> **NCT03211039** · NA · UNKNOWN · sponsor: **Rady Pediatric Genomics & Systems Medicine Institute** · enrollment: 213 (actual)

## Conditions studied

- Genetic Diseases
- Genetic Syndrome
- Mendelian Disorders

## Interventions

- **GENETIC:** Genomic sequencing and molecular diagnostic results, if any.

## Key facts

- **NCT ID:** NCT03211039
- **Lead sponsor:** Rady Pediatric Genomics & Systems Medicine Institute
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2017-06-29
- **Primary completion:** 2018-10-09
- **Final completion:** 2024-07-30
- **Target enrollment:** 213 (ACTUAL)
- **Last updated:** 2024-03-01

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03211039

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03211039, "Perinatal Precision Medicine". Retrieved via AI Analytics 2026-06-12 from https://api.ai-analytics.org/clinical/NCT03211039. Licensed CC0.

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