Clinical Trial

Timing of Thromboprophylaxis After Postpartum Hemorrhage

Completed
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Summary
Postpartum hemorrhage is a leading cause of maternal morbidity and mortality worldwide. Women who experience severe postpartum hemorrhage are at increased risk of both recurrent bleeding and venous thromboembolism. The optimal timing for starting pharmacological thromboprophylaxis after postpartum hemorrhage remains uncertain. This retrospective observational cohort study was conducted at the Center of Maternity and Neonatology of Tunis, Tunisia. The study included women who experienced postpartum hemorrhage between 2018 and 2024 and received pharmacological thromboprophylaxis during the postpartum period. The objective was to evaluate the association between the timing of thromboprophylaxis initiation and the occurrence of thromboembolic and hemorrhagic complications. The findings are expected to contribute to the optimization of thromboprophylaxis timing after postpartum hemorrhage and to improve the balance between the prevention of venous thromboembolism and the risk of recurrent bleeding.
Trial Details
NCT Number NCT07689136
Lead Sponsor University Tunis El Manar
Conditions Postpartum Hemorrhage, Venous Thromboembolism, Pulmonary Embolism, Deep Vein Thrombosis
Enrollment 236 participants
Start Date 2025-03-01
Primary Completion 2025-03-01 (estimated)
Study Completion 2025-03-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-08