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OpenTrials
Completed

NCT Number: NCT05530616

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

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.

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Key information

Conditions

Fetal Weight Body Weight Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Service de Gynécologie Obstétrique - CHU de Strasbourg - France

Strasbourg, 67091, France

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. 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.

    Time frame: Files analysed retrospectively from January 01, 2000 to December 31, 2021 will be examined

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Registry information

Acronym: EPF

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 7, 2022
Registry last updated
Nov 9, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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