Obstetric anaesthesia

Prophylactic tranexamic acid for the prevention of postpartum haemorrhage in women with placenta praevia: multicentre, double blind, randomised, placebo controlled, phase 3 trial

BMJPublished Randomised controlled trial

Primary resultResult — go to the resultRelative risk 0.85 95.2% CI 0.75–0.96

Authors' conclusion

In women with placenta praevia who underwent caesarean delivery and received prophylactic oxytocin, treatment with tranexamic acid resulted in a statistically significant yet modest reduction in the incidence of postpartum haemorrhage, with no signal of increased serious adverse events.

Study context

Population
Women with placenta praevia undergoing caesarean delivery, 24 maternity units across China, July 2023–March 20251,691 with primary outcome data
Participants
1,732 women
Comparison
Prophylactic TXA vs placebo, with prophylactic oxytocin
  • Tranexamic acidn = 845
  • Placebon = 846reference
Primary endpoint
PPH: calculated estimated blood loss ≥1000 mL or red cell transfusion
Follow-up
Within two days after delivery
Methodological detailsmulticentre, double blind, placebo controlled, phase 3, 38 excluded after randomisation (withdrew consent or ineligible)
  • Multicentre
  • Double blind
  • Placebo controlled
  • Phase 3
  • 38 excluded after randomisation (withdrew consent or ineligible)

Primary result

As reported in the abstract

Relative risk

0.85

95.2% CI 0.75–0.96

P = 0.01

Events by treatment group

Tranexamic acid vs Placebo
RR 0.85 (95.2% CI 0.75–0.96); P = 0.01

Further findings

Placenta accreta spectrum diagnosed in 303 participants
17.9%

Safety

OutcomeTranexamic acidPlaceboRR (95% CI)
Serious adverse events (thromboembolic events, seizures, acute kidney or liver injury, maternal death)Similar between groups0.5%0.5%1.01 (0.25–4.00)

Original publication

Prophylactic tranexamic acid for the prevention of postpartum haemorrhage in women with placenta praevia: multicentre, double blind, randomised, placebo controlled, phase 3 trial. BMJ. Published 13 May 2026. doi:10.1136/bmj-2026-089636

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