high-risk postpartum haemorrhage women undergoing caesarean section
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All consenting women with the following: Previous history of PPH Previous caesarean section Coexisting uterine fibroid Macrosomia Polyhydramnios Placenta praevia Mild abruptio placentae Multiple pregnancy Preeclampsia Eclampsia Failed induction or augmentation of labour Placenta accreta spectrum
Exclusion criteria
Exclusion criteria: Disseminated intravascular coagulopathy Known allergy to tranexamic acid
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean blood loss in both arms of the study during surgery, up to 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| The proportion of women who will need blood transfusion in both arms of the study. The proportion of women in both arms who will require additional uterotonic(s) and surgical interventions. Proportion of primary PPH in both arms of the study after surgery Proportion of postpartum maternal anaemia in both arms of the study after surgery | — |
Countries
Nigeria
Contacts
Postgraduate student