RecruitingNot ApplicableNCT03659708

Pregnancy and Risk of Venous Thromboembolism

Prospective Multicentre Randomized Clinical Trial on the Management of Pregnancies With High Risk of Venous Thrombosis


Sponsor

Hospices Civils de Lyon

Enrollment

600 participants

Start Date

Jan 22, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

The management of venous thromboembolism (VTE) risk in pregnancy still remains a challenge. An individual assessment of the VTE risk is crucial for optimal thromboprophylaxis, but there is no validated tool to help clinicians stratify the risk in pregnant women and introduce prophylactic anticoagulation at the appropriate time. Recommendations mostly based on case-control studies and expert opinions do not accurately reflect the physician's need. In view of the lack of international recommendations with a high level of evidence regarding prophylactic treatment of pregnant women at risk of thrombosis, the use of a risk stratification tool that takes all individual risk factors for VTE into consideration and which aids decisions over prophylaxis regimens may help. Investigators have previously described a VTE risk score (the Lyon-VTE-score), rating patients at increased risk of VTE and recommending individually tailored management. A retrospective evaluation of the initial score showed favorable outcomes in pregnancies with a high risk of thrombosis. A subsequent multicenter prospective study reported promising results using this score and related management strategy. The efficacy and safety after 10 years of prospective use of the Lyon-VTE-score in daily practice to guide the prescription of antithrombotic prophylaxis during pregnancy was recently evaluated and the results showed that the Lyon-VTE-score allows a standardized approach with objective criteria and can help non-specialized centers and young doctors manage these high-risk pregnancies. The results of previous studies provide consistent conclusions on the safety and efficacy of the approach of investigators and give background for a medico-economic study to evaluate costs and consequences of this procedure. The most recent study (2005) evaluating the cost of prophylaxis in pregnant women, evaluated this cost as $1292 for each 6-week cycle of treatment. In addition, the use of such a score offers the prospect of personalized medicine, which is probably more cost-efficient compared to "inclusive, equal treatment for all". In antepartum, the decision to administer thromboprophylaxis should be considered on an individual basis with regard to lowering the absolute risk of thrombosis, the inconvenience of daily subcutaneous heparin therapy and the potential risks of bleeding, heparin-induced thrombocytopenia and osteoporosis. An individual assessment of the VTE risk is crucial for optimal thromboprophylaxis, but there is no validated tool to help clinicians to stratify VTE risk in pregnant women and to introduce prophylactic anticoagulation at the right time. Most of the recommendations are grade 2C. They are mostly based on case-control studies and expert opinions and do not entirely highlight the physicians' need. The originality of this approach is the use of a risk stratification tool that takes all individual risk factors for VTE into consideration and that aids the decision-making process of antenatal anti-thrombotic prophylaxis. This study will personalize care using a score to individually assess the risk and propose appropriate prevention. The main objective of this study is to conduct a medico-economic study to evaluate the efficiency of an innovative strategy integrating the Lyon-VTE-score in the management of pregnant patients with venous thromboembolism risk versus standard care.


Eligibility

Min Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This study follows pregnant women who are at high risk of developing blood clots (venous thromboembolism, or VTE) during their pregnancy. These are women who have had a blood clot before or who have a clotting disorder (thrombophilia). The study is observational — it tracks outcomes and treatment decisions rather than testing a new drug — to help doctors better understand how to manage VTE risk during pregnancy. Managing blood clots in pregnancy is complex: anticoagulant medications (blood thinners like heparin) carry risks for both mother and baby, and the evidence base for optimal dosing and timing is still evolving. This study aims to contribute to that evidence. You may be eligible if: - You are a pregnant adult woman (18 to 50 years) - You are at high risk of VTE with a personal history of blood clots and/or thrombophilia - You have given informed consent to participate You may NOT be eligible if: - You have a contraindication to heparin therapy - You have obstetric complications only (no personal VTE history) - You have a history of only superficial vein thrombosis - You are already on long-term anticoagulants, or have antiphospholipid syndrome or antithrombin deficiency - You are participating in another study that could interfere with this one Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURELyon-VTE score

follow-up at 3 months, 5 months, 7 months during pregnancy and 3 months and 12 months after delivery.

PROCEDURErecommendations currently available

follow-up at 7 months during pregnancy and 3 months and 12 months after delivery.


Locations(1)

Hôpital Cardiologique L. Pradel

Bron, France

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NCT03659708


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