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The purpose of this study is to evaluate using the recent consensus based definition for FGR using biometric and Doppler parameters to identify fetuses at risk of adverse perinatal outcomes compared to using solely biometric based parameter (EFW <10th percentile according to the Hadlock growth standard).
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Inclusion criteria
Participants included in this study will have the following criteria:
Exclusion criteria
• Fetal structural malformations or chromosomal abnormalities as detected by neonatal examination and anomaly scan during pregnancy.
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Central trial contact
Radwa Rasheedy, MD
Data sourced from clinicaltrials.gov
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