← Eichor
Study identifier: NCT06845423 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Prevention of Postpartum Venous Thromboembolism in Women at Intermediate Risk

Condition: Venous Thromboembolism (VTE) · Post Partum Women  ·  Sponsor: University Hospital, Brest

PhasePhase 4
Planned participants2400
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Venous thromboembolism (VTE) is currently the second cause of death in women of reproductive age worldwide. The incidence of VTE during pregnancy is 1.2 to 1.4/1000 women, half of VTE occurring during postpartum and as PE in majority of cases, accounting for 8.8% of maternal deaths. Majority of postpartum VTE occurs in women with one or more moderate risk factors (obesity, caesarean section, postpartum hemorrhage). For these women at intermediate risk, the efficacy and safety of thromboprophylaxis have not been assessed yet during postpartum and international guidelines for pharmacological thromboprophylaxis, based on data extrapolated from other populations, observational studies and small clinical trials are inconsistent across countries. We designed an open-label, randomized, controlled trial, aiming to demonstrate the superiority of a pharmacological thromboprophylaxis strategy with LMWH (LMWH type chosen according to physician / patient's preference) during 6 weeks after delivery (the 6-weeks follow-up visit being matched with usual care) in women at intermediate risk, over no pharmacological thromboprophylaxis.

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

Talk to the study team

Emmanuelle LE MOIGNE, MD, PhD  ·  0298347344  ·  emmanuelle.lemoigne@chu-brest.fr

Sarah ROBIN, MD  ·  sarah.robin@chu-brest.fr

Always discuss trial participation with your own doctor first.

Locations (18)

CHU d'Amiens PicardieAmiens, FranceNot Yet Recruiting
CHU de Bordeaux, Groupe Pellegrin, Centre Aliénor d'AquitaineBordeaux, FranceNot Yet Recruiting
CHU de BrestBrest, FranceRecruiting
Hôpital Béclère, AP-HPClamart, FranceNot Yet Recruiting
CHU de Clermont Ferrand Site EstaingClermont-Ferrand, FranceNot Yet Recruiting
CH départemental de VendéeLa Roche-sur-Yon, FranceNot Yet Recruiting
Hôpital Bicêtre, AP-HPLe Kremlin-Bicêtre, FranceNot Yet Recruiting
Hôpital Nord Marseille, AP-HMMarseille, FranceNot Yet Recruiting
Centre Hospitalier des Pays de MorlaixMorlaix, FranceNot Yet Recruiting
CHRU de NancyNancy, FranceNot Yet Recruiting
CHU de NantesNantes, FranceNot Yet Recruiting
Hôpital Lariboisière, AP-HPParis, FranceNot Yet Recruiting

+ 6 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06845423