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NCT05551078 Clinical Trial

Thrombophilia Screening After Severe IUGR

Pregnancy Complications Clinical Trial

Official title:
Thrombophilia Screening in Women After Severe IUGR

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05551078
Other study ID # 2022PI102
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 15, 2022
Est. completion date January 2023

Study information
Verified date September 2022
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date January 2023
Est. primary completion date October 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Women over 18 years old - Pregnant women - IUGR defined by an EFW <3rd centile - IUGR before 25 GW Exclusion Criteria: - none

Study Design

Related Conditions & MeSH terms

Intervention

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

Locations
Country Name City State
France Matthieu Dap Nancy

Sponsors (1)
Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of positive's thrombophilia screening 5 years
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