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Study identifier: NCT07140211 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Short-term Low-dose Low-molecular-weight Heparin to Prevent Postpartum Thrombosis

Condition: Venous Thromboembolism (VTE) · Postpartum  ·  Sponsor: Marc Blondon

PhasePhase 3
Planned participants9200
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Marc Blondon  ·  (+41).22.372.92.92  ·  marc.blondon@hug.ch

Always discuss trial participation with your own doctor first.

Locations (8)

Kantonsspital BadenBaden, SwitzerlandRecruiting
Universitätsspital BaselBasel, SwitzerlandRecruiting
LindenhofspitalBern, SwitzerlandRecruiting
Geneva University HospitalsGeneva, SwitzerlandRecruiting
Centre Hospitalier Universitaire VaudoisLausanne, SwitzerlandRecruiting
Ente Ospedaliero CantonaleLugano, SwitzerlandRecruiting
Réseau Hospitalier NeuchâteloisNeuchâtel, SwitzerlandRecruiting
Hôpital du ValaisSion, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT07140211