CClinicalTrials.gg
Status unknownNCT05551078Updated Sep 22, 2022

Thrombophilia Screening After Severe IUGR

An observational study in IUGR, Thrombophilia and Pregnancy Complications, sponsored by Central Hospital, Nancy, France. Status unknown at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-09-22.

Sponsored by Central Hospital, Nancy, France · Observational

The sponsor has not verified this record recently (last verified Sep 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
100
Ages
18 Years and older
Sex
Female
01

Study summary

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

02

Conditions studied

  • IUGR
  • Thrombophilia
  • Pregnancy Complications
03

In context

Pregnancy Complications

437 studies on the registry are indexed under Pregnancy Complications; 119 are open to participants now.

This study's planned enrollment of 100 is below the median of 320 across 205 observational studies indexed under Pregnancy Complications.

Browse Pregnancy Complications studies →

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • pregnant women with severe IUGR

    Biological: thrombophilia screening

Interventions

  • Biologicalthrombophilia screening

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

06

What researchers measure

Primary outcomes

  1. Rate of positive's thrombophilia screening

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
  • Matthieu Dap
    Nancy, 54000, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05551078
Lead sponsor
Central Hospital, Nancy, France
Responsible party
Sponsor
First posted
Sep 22, 2022
Start date
Sep 15, 2022
Primary completion
Oct 2022 (estimated)
Completion
Jan 2023 (estimated)
Last update
Sep 22, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.

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