Prevention of Postpartum Venous Thromboembolism in Women at Intermediate Risk. An Open-label, Randomized, Controlled Trial Comparing Two Strategies With or Without Pharmacological Thromboprophylaxis

Status: Recruiting
Location: See all (18) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women at intermediate risk of VTE during post-partum= with a 3% or more risk of VTE based on a validated prediction model\* or International guidelines (ACCP 2012).

• Age over 18 years

• Delivery between 6 hours and \< 36 hours

• Written informed consent

⁃ Definition: Intermediate risk is defined as ≥ 3%, based on risk prediction model developed by Sultan et al taking in account: smoking, varicose veins, obesity, comorbidities, diabetes, pre-eclampsia, post-partum hemorrhage, postpartum infection, emergency or elective section or following ACCP guidelines: one major risk factor or two minor risk factors.

Locations
Other Locations
France
CHU d'Amiens Picardie
NOT_YET_RECRUITING
Amiens
CHU de Bordeaux, Groupe Pellegrin, Centre Aliénor d'Aquitaine
NOT_YET_RECRUITING
Bordeaux
CHU de Brest
RECRUITING
Brest
Hôpital Béclère, AP-HP
NOT_YET_RECRUITING
Clamart
CHU de Clermont Ferrand Site Estaing
NOT_YET_RECRUITING
Clermont-ferrand
CH départemental de Vendée
NOT_YET_RECRUITING
La Roche-sur-yon
Hôpital Bicêtre, AP-HP
NOT_YET_RECRUITING
Le Kremlin-bicêtre
Hôpital Nord Marseille, AP-HM
NOT_YET_RECRUITING
Marseille
Centre Hospitalier des Pays de Morlaix
NOT_YET_RECRUITING
Morlaix
CHRU de Nancy
NOT_YET_RECRUITING
Nancy
CHU de Nantes
NOT_YET_RECRUITING
Nantes
Groupe Hospitalier Paris Saint Joseph
NOT_YET_RECRUITING
Paris
Hôpital Lariboisière, AP-HP
NOT_YET_RECRUITING
Paris
CH de Pau
NOT_YET_RECRUITING
Pau
Centre Hospitalier de Périgueux
NOT_YET_RECRUITING
Périgueux
Centre Hospitalier de Cornouaille Quimper Concarneau
NOT_YET_RECRUITING
Quimper
CHU de Rennes
NOT_YET_RECRUITING
Rennes
CHU de St Etienne - Hôpital Nord
NOT_YET_RECRUITING
Saint-priest-en-jarez
Contact Information
Primary
Emmanuelle LE MOIGNE, MD, PhD
emmanuelle.lemoigne@chu-brest.fr
0298347344
Backup
Sarah ROBIN, MD
sarah.robin@chu-brest.fr
Time Frame
Start Date: 2025-05-16
Estimated Completion Date: 2028-08-16
Participants
Target number of participants: 2400
Treatments
Experimental: Experimental Group
Pharmacological thromboprophylaxis using LMWH at preventive dosage. The choice of subcutaneous LMWH depends on the practice of each center:~* Enoxaparine 4000 UI (weight \> 90 kg 6000 UI)~* Tinzaparine 3500 UI (weight \> 90 kg 4500 UI)~* Dalteparine 5000 UI (weight \> 90 kg 7500 UI)~* Nadroparine 2850 UI (weight \> 90 kg 3800 UI).~All patients can have compression stockings
No_intervention: Control group
No pharmacological thromboprophylaxis. All patients can have compression stockings.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Brest

This content was sourced from clinicaltrials.gov