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impact of tranexamic acid on the prevention of during and post-caesarean hemorrhage

impact of tranexamic acid on the prevention of hemorrhage during and after cesarean section in parturients at risk.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202108668389918
Enrollment
796
Registered
2021-08-24
Start date
2019-09-03
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Haematological Disorders Pregnancy and Childbirth Surgery post partum hemorhage

Interventions

tranexamic acid prophylaxis to reduce postpartum hemorrhage in vulnerable parturients
intervention without active ingredient or therapeutic effect

Sponsors

University Hospital Lamine Debaghine Bab El Oued
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: - Scheduled or semi-emergency cesarean section. - Live fetus. - Gestational age greater than or equal to 35 SA. - Parturients classified as ASA I or ??,consenting, with 2 or more risk factors for postpartum hemorrhage: * polyhydramnios. * age greater than 35 years. * Fetal macrosomia. * coagulation anomaly. * thrombopenia. * anticoagulant treatment. * antecedents of postpartum hemorrhage. * placenta pravea not recovering. * Anemia. * Pre-eclampsia. * Multiple pregnancy. * Multiple pregnancy. * Chorioamniotitis.

Exclusion criteria

Exclusion criteria: - Allergy to tranexamic acid. - Severe renal impairment. - History of thrombosis. - Epilepsy. - Death in utero - Severe medical or surgical complication involving the heart, liver, kidneys, or brain. - Placental insertion anomalies: placenta accreta and covering pravea. - Caesarean sections performed for active bleeding during uterine rupture, retro placental hematoma, or placenta previa.

Design outcomes

Primary

MeasureTime frame
There was statistically significant reduction in the mean blood loss among the study group who received tranexamique acid in comparison to the control group

Secondary

MeasureTime frame
no major side effects

Countries

Algeria

Contacts

Public Contacthouda Ghabouli

resident physician

houdadoudada@gmail.com+21323156680

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026