Health Condition 1: null- Pregnant women planned for cesarean delivery
Conditions
Interventions
Intervention1: Tranexamic acid: 10 mg / kg diluted to 20 ml with normal saline given IV 10 min prior to skin incision
Control Intervention1: Normal saline: 20 ml given IV 10 min prior to skin incision
Sponsors
Max Super Speciality Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Pregnant women at high risk for bleeding planned for cesarean delivery.
Exclusion criteria
Exclusion criteria: history of ischemic cardiac disease, hemodynamic instability before commencement of surgery, bleeding disorders, known allergy to tranexamic acid, history of any thrombogenic episodes, patients on anticoagulants history of kidney disease history of hematuria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to find the need for additional uterotonic drugs in the first 24 hours postpartum in women at increased risk for obstetric hemorrhageTimepoint: from start of cesarean section till 24 hours after baby delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives were to compare between the two groups the estimated blood loss, requirement for blood transfusion, any neonatal adverse events or thrombogenic episodes in the mother.Timepoint: from start of cesarean section till 24 hours after baby delivery | — |
Countries
India
Contacts
Public ContactNambiath Sujata
Department of Anesthesiology, Max Super Speciality Hospital
Outcome results
None listed