Actively Recruiting
Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
Led by Guangzhou Women and Children's Medical Center · Updated on 2019-06-04
10000
Participants Needed
1
Research Sites
982 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women presenting at Guangzhou Women and Children's Medical Center with prenatal diagnosis of intrauterine growth restriction (IUGR), structural anomaly, or chromosomal anomaly
- Neonates or infants diagnosed with intrauterine growth restriction (IUGR), structural anomaly, or chromosomal anomaly
You will not qualify if you...
- Pregnant women who do not agree to participate
- Pregnant women delivering babies at other hospitals
- Cases with prenatally suspected anomalies not confirmed by postnatal diagnosis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Guangzhou Women and Children's Medical Center
Guangzhou, Guangdong, China, 510623
Actively Recruiting
Research Team
W
Wei Zhong, Master
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here