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Search / Trial NCT06575309

THROmbinography in Pregnant Woman and in Vitro Action of Low Molecular Weight HEparin

Launched by UNIVERSITY HOSPITAL, CLERMONT-FERRAND · Aug 26, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Thrombography Pregnancy Postpartum Low Molecular Weight Heparins (Lmwh)

ClinConnect Summary

This clinical trial, titled "THROmbinography in Pregnant Women and in Vitro Action of Low Molecular Weight Heparin," is studying how pregnancy affects blood clotting and the use of a medication called low-molecular-weight heparin (LMWH) to prevent blood clots in pregnant women. During pregnancy, women's bodies undergo significant changes that can lead to a higher risk of blood clots, especially in the legs or lungs. The researchers want to understand how LMWH works in pregnant women compared to non-pregnant women, as well as how it affects clotting during different stages of pregnancy and after childbirth.

To participate in this trial, women must be in their first trimester of a normal pregnancy and be over 18 years old. However, those with certain health conditions, such as known blood clotting disorders or a history of blood clots, cannot join. Participants will have their blood tested to measure how well it clots before and after receiving LMWH in a lab setting. This study aims to gather important information that could help doctors determine the best dose of LMWH for pregnant women to ensure their safety and well-being during and after pregnancy.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Normal 1st trimester pregnancy
  • Age \> 18
  • Exclusion Criteria:
  • Coagulation disease (Von Willebrand disease, known coagulation factor deficiency before pregnancy)
  • VTE history
  • First-degree family history of idiopathic VTE
  • Known biological risk factor for thrombosis Inherited deficiencies in coagulation inhibitors (antithrombin, protein C, protein S) Factor V Leiden polymorphism Prothrombin gene 20210G\>A polymorphism Anti-phospholipid antibodies
  • Current anticoagulant use (VKA, heparins, etc.)
  • Gestational diabetes detected in the 1st trimester
  • Pre-existing type 1 and type 2 diabetes
  • History of pathological pregnancy Premature delivery Postpartum hemorrhage Preeclampsia
  • Hepatopathy
  • Obesity (BMI ≥ 30)
  • Infections (HIV, HBV, HCV...)
  • Autoimmune diseases
  • Pregnancy resulting from in vitro fertilization protocol
  • Multiple pregnancy
  • Patient under guardianship, curatorship or safeguard of justice
  • Patient not covered by a social security scheme
  • Patient deprived of liberty

About University Hospital, Clermont Ferrand

The University Hospital of Clermont-Ferrand is a leading academic medical institution dedicated to advancing healthcare through innovative research and clinical trials. Renowned for its multidisciplinary approach, the hospital integrates cutting-edge scientific inquiry with patient care, fostering an environment that promotes collaboration among healthcare professionals, researchers, and academic partners. With a strong commitment to improving patient outcomes, the institution actively engages in a wide array of clinical studies, ranging from early-phase trials to large-scale interventions, aimed at addressing critical health challenges and enhancing treatment modalities. Its state-of-the-art facilities and expertise make it a pivotal contributor to clinical research in the region and beyond.

Locations

Clermont Ferrand, , France

Clermont Ferrand, , France

Patients applied

0 patients applied

Trial Officials

Aurélien Lebreton

Principal Investigator

CHU de Clermont-Ferrand

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported