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The China Neonatal Genomes Project

NCT03931707 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100000

Last updated 2026-03-16

No results posted yet for this study

Summary

The project will carry out the genetic testing of 100000 neonates in the next 5 years. The aim of the project is to construct the Chinese neonatal genome database, establish the genetic testing standard of neonatal genetic diseases, and promote the industrialization of neonatal genetic disease gene testing, improve the training system for genetic counseling.

Conditions

  • Newborn
  • Hereditary Disease
  • Genetic Predisposition to Disease
  • Defect, Congenital

Interventions

GENETIC

Genomic sequencing

Both sick and high-risk newborn un-randomized to receive genomic sequencing will receive a Genomic Newborn Sequencing Report which will include pathogenic or likely pathogenic variants identified in genes associated with childhood-onset disease.

Sponsors & Collaborators

  • Children's Hospital of Fudan University

    lead OTHER

Principal Investigators

  • Wenhao Zhou · Children's Hospital of Fudan University

Eligibility

Max Age
28 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-08
Primary Completion
2026-12-30
Completion
2026-12-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03931707 on ClinicalTrials.gov