Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 18
SponsorGuangzhou Women and Children's Medical Center
About this trial
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.
Eligibility criteria
Qualifiers
Intrauterine growth restriction (IUGR)
Structural anomaly
Chromosomal anomaly
Disqualifiers
Pregnant women who don't agree to participate;
Pregnant women delivering babies at other hospitals.
Prenatally suspected anomalies that are not confirmed by postnatal diagnosis.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
10,000 Participants
are grouped into 3 trial groupsSponsors and collaborators
Source ClinicalTrials.gov