Fetal biometry in pregnancy
Conditions
Interventions
Group 1: All pregnant patients admitted to the hospital up to 3 days before delivery.
Sponsors
Uniklinikum Frankfurt
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Singleton, monochorionic diamnotic (MCDA) and dichorionic diamniotic (DCDA) twin pregnancies between 28+0 and 42+0 weeks of gestation
Exclusion criteria
Exclusion criteria: Monochorionic monoamniotic twin pregnancies Indication for immediate delivery Major fetal structural anomalies or aneuploidies Oligohydramnios/anhydramnios Unable to give informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study is to assess the accuracy of automated AI-assisted measurement of EFW versus measurement of EFW performed manually by trained clinicians on ultrasound, within 3 days before delivery, in comparison to birthweight. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives of this study include: - Comparison of fetal biometry (BPD, HC, AC, FL) in singleton and twin pregnancies between automated AI-assisted and manual biometric measurements. - Comparison of the accuracy of manual biometric measurements with birthweight performed by operators with different levels of experience, and subanalysis of the AI- assisted biometric measurements based on operator experience. - Determination of factors influencing the accuracy and duration of ultrasound estimation of fetal weight compared between AI-assisted automated ultrasound measurement technique and manual ultrasound measurements (e.g. maternal body mass index (BMI), ethnicity, etc). | — |
Countries
Australia, France, Germany, Italy, Spain, United Kingdom, United States
Contacts
Public ContactEileen Deuster
Universitätsklinikum Frankfurt
Outcome results
None listed