Thrombophilia Screening After Severe IUGR

Overview

This retrospective study aims to assess the input of thrombophilia screening in pregnant women with severe intra-uterine growth restricted babies.

Full Title of Study: “Thrombophilia Screening in Women After Severe IUGR”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Retrospective
  • Study Primary Completion Date: October 2022

Interventions

  • Biological: thrombophilia screening
    • In the IUGR group systematic thrombophilia screening had already been performed.

Arms, Groups and Cohorts

  • pregnant women with severe IUGR

Clinical Trial Outcome Measures

Primary Measures

  • Rate of positive’s thrombophilia screening
    • Time Frame: 5 years

Participating in This Clinical Trial

Inclusion Criteria

  • Women over 18 years old – Pregnant women – IUGR defined by an EFW <3rd centile – IUGR before 25 GW Exclusion Criteria:

  • none

Gender Eligibility: Female

Pregnant women

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Central Hospital, Nancy, France
  • Provider of Information About this Clinical Study
    • Sponsor

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