FGR Diagnostic Criteria in Predicting Adverse Neonatal Outcomes

• Conditions: FGR

• Registration Number: NCT04933396
• Lead Sponsor: Ain Shams University

Brief Summary

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).

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-06
• Study First Submitted: 2021-06-17
• Study First Submitted QC: 2021-06-18
• Last Update Submitted: 2021-06-18
• Study First Posted: 2021-06-21
• Last Update Posted: 2021-06-21
• Study Start: 2021-07-01
• Primary Completion: 2021-12-01
• Study Completion: 2021-12-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

• Participants included in this study will have the following criteria:

  • Pregnancies complicated with FGR (EFW <10th percentile).
  • Singleton pregnancy.

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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.

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
adverse events	30 days after delivery	neonatal outcome

Trial Locations

Locations (1)

Ain Shams university maternity hospital; 🇪🇬 Cairo, Egypt