FGR Diagnostic Criteria in Predicting Adverse Neonatal Outcomes

Ain Shams University50 enrolled

Overview

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).

Study Type

OBSERVATIONAL

Enrollment

Conditions

FGR

Interventions

ultrasound diagnostic criteriaDIAGNOSTIC_TEST

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).

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: * Participants included in this study will have the following criteria: * Pregnancies complicated with FGR (EFW \<10th percentile). * Singleton pregnancy. Exclusion Criteria: * • Fetal structural malformations or chromosomal abnormalities as detected by neonatal examination and anomaly scan during pregnancy. * Identified infectious etiologies detected during immediate postnatal examination or during pregnancy. * Gestational age cannot be calculated accurately. * Missing antenatal or perinatal outcome data.

Locations (1)

Ain Shams university maternity hospital

Cairo, Egypt

Outcomes

Primary Outcomes

adverse events

neonatal outcome

Time frame: 30 days after delivery

Central Contacts

Radwa Rasheedy, MD

CONTACT

01283492979 radwaebed@yahoo.com

Data from ClinicalTrials.gov

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