Overview

The Efficacy of Tranexamic Acid in Preventing Postpartum Haemorrhage After Caesarean Section

Status:
Recruiting
Trial end date:
2021-12-31
Target enrollment:
0
Participant gender:
Female
Summary
This study seeks to determine if the using tranexamic acid prophylactically at caesarean section will prevent postpartum haemorrhage which is a major cause of maternal mortality in Zimbabwe and globally.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Zimbabwe
Collaborator:
Fogarty International Center of the National Institute of Health
Treatments:
Tranexamic Acid
Criteria
Inclusion Criteria: Women undergoing elective or emergency caesarean section with:

- Estimated gestational age of 37 weeks or more

- Live intrauterine foetus

- Elective or emergency caesarean delivery

- Signed informed consent

Exclusion Criteria:

- History of coagulopathies or conditions predisposing them to thromboembolic phenomena,

- seizure history,

- autoimmune disease,

- placental abruption,

- placenta praevia,

- abnormally adherent placentae if identified on prenatal ultrasound,

- eclampsia or HELLP syndrome,

- known hypersensitivity to TXA,

- planned general anaesthesia,

- caesarean delivery for the second twin or second/third triplet(s) after vaginal birth
of the first twin,

- poor understanding of English/Shona languages,

- those who have received anticoagulants in the week before delivery

- persons-under-investigation for Coronavirus disease (COVID-19) and confirmed COVID-19
positive women