Overview
The Efficacy of Tranexamic Acid in Preventing Postpartum Haemorrhage After Caesarean Section
Status:
Recruiting
Recruiting
Trial end date:
2021-12-31
2021-12-31
Target enrollment:
0
0
Participant gender:
Female
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 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of ZimbabweCollaborator:
Fogarty International Center of the National Institute of HealthTreatments:
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