Million-Baby gene study aims to unlock secrets of genetic disease
NCT ID NCT07365254
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will enroll up to 1 million families to collect genetic and health information from parents and newborns. Researchers will analyze whole genomes, blood markers, and other biological data to understand how genes and environment affect pregnancy and child health. The goal is to find new ways to predict and prevent genetic diseases early in life.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this could help identify genetic risks early in life and improve prevention of birth defects and childhood diseases.
- What could go wrong
- This is an observational study, not a treatment trial. It may not lead to direct medical benefits, and results may take many years to apply.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Women's Hospital, School of Medicine, Zhejiang University
RECRUITINGHangzhou, Zhejiang, 310006, China
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Other studies related to the condition(s) this trial covers.
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