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FGR Diagnostic Criteria in Predicting Adverse Neonatal Outcomes

A

Ain Shams University

Status

Unknown

Conditions

FGR

Treatments

Diagnostic Test: ultrasound diagnostic criteria

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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).

Enrollment

50 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Radwa Rasheedy, MD

Data sourced from clinicaltrials.gov

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