Prevention of Postpartum Venous Thromboembolism in Women at Intermediate Risk
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.
Timeline
- Start
- 2025-05-16
- Primary completion
- 2028-05-16
- Completion
- 2028-08-16
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Dalteparin sodium | Other / unclassified | 2850 iu | Subcutaneous |
| Subject | Dalteparin sodium | Other / unclassified | 3800 iu | Subcutaneous |
| Subject | Dalteparin sodium | Other / unclassified | 5000 iu | Subcutaneous |
| Subject | Dalteparin sodium | Other / unclassified | 7500 iu | Subcutaneous |
| Subject | Enoxaparin sodium | Other / unclassified | 3500 iu | Subcutaneous |
| Subject | Enoxaparin sodium | Other / unclassified | 4000 iu | Subcutaneous |
| Subject | Enoxaparin sodium | Other / unclassified | 4500 iu | Subcutaneous |
| Subject | Enoxaparin sodium | Other / unclassified | 6000 iu | Subcutaneous |