Status: Recruiting
Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
The purpose of this prospective cohort study is to build a large platform that includes clinical information (prenatal diagnosis and postnatal follow-up data) and biological specimen banks of fetuses/infants with IUGR or congenital anomalies, which provide vital support and research foundation for accurate diagnosis, precision treatment and meticulous management.
Participants needed: 10,000
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Guangzhou Women and Children's Medical CenterUpdated: Jun 4, 2019Locations: 1Duration: 20 Years
Eligibility criteria
Intrauterine growth restriction (IUGR) [+2]
Pregnant women who don't agree to participate; [+2]