# Whole Exome Screening of Newborns

> **NCT05325749** · — · UNKNOWN · sponsor: **Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare** · enrollment: 7000 (estimated)

## Conditions studied

- Infant, Newborn

## Interventions

- **GENETIC:** Screening
- **GENETIC:** Family history record
- **OTHER:** Questionnaire survey
- **GENETIC:** Diagnostic
- **GENETIC:** Selective screening

## Key facts

- **NCT ID:** NCT05325749
- **Lead sponsor:** Federal State Budget Institution Research Center for Obstetrics, Gynecology and Perinatology Ministry of Healthcare
- **Sponsor class:** OTHER_GOV
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2021-07-10
- **Primary completion:** 2022-12
- **Final completion:** 2022-12
- **Target enrollment:** 7000 (ESTIMATED)
- **Last updated:** 2022-04-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05325749

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05325749, "Whole Exome Screening of Newborns". Retrieved via AI Analytics 2026-06-12 from https://api.ai-analytics.org/clinical/NCT05325749. Licensed CC0.

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