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Impact of Ultrasound Fetal Weight Estimation on Obstetrical Management and Maternal and Neonatal Outcomes

Impact of Ultrasound Fetal Weight Estimation on Obstetrical Management and Maternal and Neonatal Outcomes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05530616
Acronym
EPF
Enrollment
70000
Registered
2022-09-07
Start date
2022-05-13
Completion date
2023-10-13
Last updated
2023-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fetal Weight

Keywords

Fetal Weight, Ultrasound Fetal Weight, Obstetrical Management, Maternal Outcomes, Neonatal Outcomes

Brief summary

The investigators wish to study the obstetrical data of pregnant women who had an ultrasound estimation of fetal weight and who delivered at the University Hospital of Strasbourg over the last 20 years. These retrospectively collected data are a valuable source of scientific information since they are real life data, currently of growing interest in the scientific community, and have a large volume and quality due to the number of years included and the variety of information collected in the computerized media records. From this study, the investigators hope not only to better understand the consequences of ultrasound screening for fetal growth, but also to improve its accuracy and to develop useful models in obstetrical decision making in order to decrease maternal and neonatal morbidity.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum

Inclusion criteria

* Major subject (≥18 years of age). * Female and with a single pregnancy * Subject having had an ultrasound follow-up at HUS between 01/01/2000 and 31/12/2021 * Subject who gave birth at HUS between 01/01/2000 and 12/31/2021 * Subject who does not object to the reuse of her data for scientific research purposes

Exclusion criteria

* Subject who has expressed opposition to the reuse of their data for scientific research purposes * Multiple pregnancies * Delivery before 24 weeks of amenorrhea * Diagnosis of a malformative fetal pathology * Diagnosis of fetal death in utero

Design outcomes

Primary

MeasureTime frame
Retrospective study of maternal and neonatal clinical and ultrasound data for the development of an algorithm model useful in obstetrical decision making in order to decrease maternal and neonatal morbidity.Files analysed retrospectively from January 01, 2000 to December 31, 2021 will be examined

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026