# Implementation of Whole Genome Sequencing as Screening in a Diverse Cohort of Healthy Infants

> **NCT05161169** · NA · COMPLETED · sponsor: **Brigham and Women's Hospital** · enrollment: 500 (actual)

## Conditions studied

- Genetic Predisposition to Disease
- Hereditary Diseases

## Interventions

- **GENETIC:** Genome Sequencing

## Key facts

- **NCT ID:** NCT05161169
- **Lead sponsor:** Brigham and Women's Hospital
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2022-12-21
- **Primary completion:** 2025-06-30
- **Final completion:** 2025-06-30
- **Target enrollment:** 500 (ACTUAL)
- **Last updated:** 2026-03-05

## Collaborators

- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05161169

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05161169, "Implementation of Whole Genome Sequencing as Screening in a Diverse Cohort of Healthy Infants". Retrieved via AI Analytics 2026-08-11 from https://api.ai-analytics.org/clinical/NCT05161169. Licensed CC0.

---

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