Clinical Trial

Trends in the Administration of Tranexamic Acid for Postpartum Hemorrhage

Recruiting
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Record status
This record was last updated December 22, 2025 (before its estimated March 31, 2026 completion). Its status may not reflect the trial's current state.
Summary
Postpartum hemorrhage (PPH) is the global leading cause of maternal death, with 20-30% of maternal deaths in Thailand linked to hemorrhage. The WOMAN Trial (2017) provided strong evidence that administering tranexamic acid (TXA)within three hours of bleeding onset lowered PPH-related mortality by 31%. Consequently, the World Health Organization (WHO) updated its guidelines, recommending TXA as part of the standard treatment package for all PPH cases. Following this, the use of TXA has been widely adopted globally and increased in Thailand. A recent study at a major Thai university hospital observed a significant increase in TXA administration after 2017. The current study aims to further analyze the recent growth rate of TXA use and its impact on obstetric and perinatal outcomes during cesarean deliveries with PPH.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-30.
Status change: Not Yet Recruiting → Recruiting 2025-12-16
Trial Details
NCT Number NCT07278037
Lead Sponsor Mahidol University
Conditions Postpartum Hemorrhage, Delivery Complication, Cesarean Section Complications, Perinatal Problems
Enrollment 648 participants
Start Date 2025-12-01
Primary Completion 2026-03-31 (estimated)
Study Completion 2026-09-30 (estimated)
Updated on ClinicalTrials.gov 2025-12-22