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Pregnancy and Fibrinogen Disorders

NCT03920332 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 149

Last updated 2022-11-02

No results posted yet for this study

Summary

The aim of this observational study is to evaluate the prevalence of uncomplicated pregnancies in women suffering from congenital fibrinogen disorders (i.e, hypofibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia) as well as to describe pregnancies outcomes in such diseases.

Conditions

  • Hypofibrinogenemia, Congenital
  • Afibrinogenemia, Congenital
  • Dysfibrinogenemia, Congenital

Sponsors & Collaborators

  • Swiss Hemophilia Network

    collaborator OTHER

  • University Hospital, Geneva

    lead OTHER

Principal Investigators

  • Alessandro Casini, MD · University Hospitals of Geneva

  • Justine Hugon-Rodin, MD, PHD · APHP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-01
Primary Completion
2022-05-01
Completion
2022-05-01

Countries

  • France
  • Slovakia
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03920332 on ClinicalTrials.gov