drugset / Trial / NCT02936661

Tranexamic Acid for Preventing Postpartum Hemorrhage After Cesarean Section

NCT02936661 ↗

Phase 4 Unknown 6700 enrolled Shanghai First Maternity and Infant Hospital
RandomizedParallel-groupQuadruple-blindPrevention

Summary

It is a multicenter randomized, double-blind and placebo-controlled trial. Totally 6500 women to delivery by cesarean section will be recruited in this study. In addition to routinely oxytocin, the women in study group will receive TXA 1 g in 2 minutes after they delivered their babies, and those in control group will receive placebo. The incidence of postpartum hemorrhage, the amount of bleeding, as well as the side effects will be observed.

Timeline

Start
2017-04
Primary completion
2018-12
Completion
2019-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Tranexamic Acid Small molecule 1 g Intravenous

Indications

No indication recorded.