Short-term Low-dose Low-molecular-weight Heparin to Prevent Postpartum Thrombosis
Sponsor: Marc Blondon • ClinicalTrials.gov ID: NCT07140211
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The goal of this clinical trial is to evaluate the risk-benefit of a short-term treatment with a low-dose low-molecular-weight heparin (LMWH), in the postpartum period (after delivery). The main questions it aims to answer are: * compared to no treatment, does short-term postpartum LMWH modify the risk of venous thromboembolism within 90 days of delivery? * compared to no treatment, does short-term postpartum LMWH modify the risks of bleeding and wound complications? Participants will take low-dose LMWH for 7-10 days or no treatment, and will be followed for 90 days post-delivery.
Interventions
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Low-dose low-molecular-weight heparin
(Drug)
Low-molecular-weight heparin given for 7-10 days after delivery: * enoxaparin 4000-6000IU o.d. * nadroparin 3800-5700IU o.d. * dalteparin 5000-7500IU o.d. * tinzaparin 4500-7000IU o.d.
Eligibility criteria
Conditions
Locations
- Kantonsspital Baden — Baden, Switzerland
- Universitätsspital Basel — Basel, Switzerland
- Lindenhofspital — Bern, Switzerland
- Geneva University Hospitals — Geneva, Switzerland
- Centre Hospitalier Universitaire Vaudois — Lausanne, Switzerland
- Luzerner Kantonspital — Lucerne, Switzerland
- Ente Ospedaliero Cantonale — Lugano, Switzerland
- Réseau Hospitalier Neuchâtelois — Neuchâtel, Switzerland
- Hôpital du Valais — Sion, Switzerland
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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