Role Of Different Prophylactic Doses Of Intravenous Tranexamic Acid In Reducing Blood Loss At Caesarean Section
Hemorrhage of Cesarean Section and/or Perineal Wound, Postpartum Hemorrhage
About this trial
This is an interventional prevention trial for Hemorrhage of Cesarean Section and/or Perineal Wound focused on measuring Caesarean Section, Tranexamic Acid, Postpartum Hemorrhage, Ecbolics
Eligibility Criteria
Inclusion Criteria:
- Maternal average age of 20-40 years.
- Singleton pregnancy at term between 38±5 days and 40 weeks.
- Elective planned or emergency secondary lower segment caesarean sections (LSCS).
Exclusion Criteria:
Women with severe medical and surgical complications as any of the following will be excluded :
- Heart, liver, kidney, or brain diseases, and blood disorders.
- Abruptio placenta, and placental abnormalities or accrete syndromes.
- Polyhydramnios, macrosomia, preeclampsia, or allergy to tranexamic acid.
- History of thromboembolic disorders, or severe anemia.
Sites / Locations
- Al-Azhar University, Faculty of Medicine for Boys ( Cairo ), Al-Hussein University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Active Comparator
Active Comparator
Active Comparator
Placebo
T1
T2
T3
Will receive a placebo (10 ml of distilled water) in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Will receive Tranexamic acid 15 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Will receive Tranexamic acid 20 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Will receive Tranexamic acid 25 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).