Methods of Placental Delivery and the Amount of Blood Loss During Cesarean Section
Complications; Cesarean Section

About this trial
This is an interventional other trial for Complications; Cesarean Section focused on measuring blood loss, caesarean section, placental delivery
Eligibility Criteria
Inclusion Criteria:
- All informed and consented women undergoing elective or emergency CS will be legible for enrollment into the study
Exclusion Criteria:
- Multiple gestation.
- Pregnancy below 34 weeks.
- Severe maternal anemia.
- Severe pre-eclampsia
- Prolonged labor.
- Prolonged rupture of the membranes with fever.
- Placental abruption.
- Placenta previa.
- Placenta accreta.
- Clotting disorders.
- Current or previous history of a significant disease including heart disease, liver, renal disorders.
Sites / Locations
- Postpartum ward of Armed Forces Hospital, Southern Region
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
manual removal group
cord traction group
Group will be assigned for manual removal of the placenta as the surgeon will introduce his hand into the uterine cavity to cleave the placenta from the decidua basalis as soon as possible after the delivery of the baby by caesarean section
Group will be assigned for controlled cord traction as the surgeon do external uterine massage and gentle traction on the exposed umbilical cord to facilitate placental delivery after the delivery of the baby by caesarean section