Estimation of Fetal Weight by Measuring Abdominal Circumference, Abdominal Subcutaneous Soft Tissue Thickness, Femur Length and Mid-thigh Soft Tissue Thickness

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorAssiut University

About this trial

Traditional methods for estimating fetal weight (EFW) often miss the mark because they focus on bone and circumference while ignoring fetal fat. This study proposes a more inclusive formula to fix that. Current models (using BPD, HC, AC, and FL) are the standard but suffer from high observer variability. These formulas struggle at the extremes (macrosomia or growth restriction) and fail to account for fetal adiposity, which makes up 10-12% of a newborn's mass. The study introduces a novel formula that moves beyond simple bone measurements by integrating Soft Tissue Thickness (STT). By accounting for a broader range of biological variants and fat distribution, this new model aims to provide a non-inferior, more precise predictive value for fetal weight compared to traditional methods.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Singleton Gestation.

Gestational Age: Participants must be at a term ≥ 37 weeks

Timing of Examination: Sonographic EFW must be performed within 48 -72 hours prior to delivery.

Welling to share in the study.

Disqualifiers

Fetal Anomalies.

Amniotic Fluid Disorders: oligohydramnios or polyhydramnios

Maternal morbid obesity (BMI > 40 kg/m2)

Maternal medical disorders: as diabetes, hypertension, systemic lupus erythromatosis or others affecting fetal growth

Trial population

full term pregnant women within 48-72 hours before delivery

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • 3rd trimester ultrasound examination within 48-72 hours of delivery

    Other intervention

    ultrasound examination of full-term pregnant women with 48-72 hours of delivery measuring Abdominal circumference, fetal abdominal subcutaneous soft tissue thickness, femur length and mid-thigh soft tissue thickness.

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: Full term pregnant women1 intervention

Trial outcomes

Primary outcomes

1

development and validation of novel method for fetal weight estimation

a novel module for fetal weight estimation depending on abdominal circumference, fetal abdominal subcutaneous soft tissue thickness, femur length, mid-thigh soft tissue thickness.

Time frame
within 48- 72 hours of delivery

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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