Randomization of Oxytocin, Oxytocin+Intrauterine Misoprostol and Carbetocin During C-section
Postpartum Hemorrhage
About this trial
This is an interventional prevention trial for Postpartum Hemorrhage focused on measuring postpartum hemorrhage, oxytocin, misoprostol, carbetocin
Eligibility Criteria
Inclusion Criteria:
- Single pregnancy greater than 37 weeks
- Pregnant women between the ages of 18-40 Volunteer
Exclusion Criteria:
- Clinical diagnosis of Gestational diabetes
- Clinical diagnosis of Gestational hypertension
- Clinical diagnosis of preeclampsia
- Clinical diagnosis of Placenta previa,
- Clinical diagnosis of abruptio placenta
- Conditions that cause excessive distention of the uterus (multiple pregnancies, severe polyhydramnios, fetal macrosomia, large fibroids displacing the cavity) Thrombophilia disorders, anticoagulation therapy History of major abdominal surgery
Sites / Locations
- Bezmialem Vakif University
- Bezmialem Vakif University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
Oxytocin Group
Oxytocin+Intrauterine Misoprostol
Carbetocin
The oxytocin infusion consisting of 20 IU dissolved in 500 mL of normal 0.9 % sodium chloride solution and infused at a rate of 125 mL/h was administered immediately after clamping the umbilical cord
The oxytocin infusion was administered immediately after clamping the umbilical cord and misoprostol tablet (400 mg) was placed into uterine cavity at the fundus after delivery of the placenta and swabbing the cavity
100-mg carbetocin was intravenously administered immediately after birth of the baby