Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
Recruiting now
Conditions studied: Intrauterine Growth Restriction, Fetal Anomaly, Chromosomal Anomalies, Pregnancy
In brief
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.
Key facts
- Study ID
- NCT03398629
- Run by
- Guangzhou Women and Children's Medical Center
- People needed
- 10000
- Starts
- 2019-05-01
- Expected to finish
- 2038-03-01
- Last updated by the study team
- 2019-06-04
Who can join
Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All pregnant women who present to Guangzhou Women and Children's Medical Center meeting one of the following prenatal diagnoses and neonates/infants who are diagnosed as one of the following anomalies will be invited to participate:
- Intrauterine growth restriction (IUGR)
- Structural anomaly
- Chromosomal anomaly
You may not qualify if…
- 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.
Where it is running
- Guangzhou Women and Children's Medical Center — Guangzhou, Guangdong, China (enrolling)
Full record on ClinicalTrials.gov
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