Uterine Cooling During Cesarean Delivery to Reduce Blood Loss and Incidence of Postpartum Hemorrhage
Postpartum Hemorrhage, Uterine Atony
About this trial
This is an interventional prevention trial for Postpartum Hemorrhage focused on measuring postpartum hemorrhage, uterine atony, cesarean section, cesarean hysterectomy, acute blood loss anemia, uterotonics, obstetric hemorrhage, severe hemorrhage, blood transfusion, obstetric emergencies, obstetrics, massive hemorrhage, hemorrhage, uterine cooling
Eligibility Criteria
Inclusion Criteria:
- Pregnant adult women of any gravidity, and gestational duration who present for cesarean section at Baylor University Medical Center in Dallas and who have given informed consent to be in the study.
Exclusion Criteria:
- Women who refuse to be in the study, and women who are unable to consent due to emergent nature of the cesarean section will be excluded. Women who are unable to understand the nature of the study due to mental illness, mental retardation, medical condition, or other communication barrier will be excluded.
- Inability to exteriorize the uterus during c-section.
Sites / Locations
- Baylor University Medical Center
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Uterine Cooling
Normal cesarean technique.
Immediately following delivery of the fetus the uterus will be externalized in the usual fashion and the body of the uterus cephalad to the hysterotomy incision will be wrapped in sterile surgical towels saturated in sterile, iced normal saline. These towels will come from a sterile cooling pot set to 30 degrees Fahrenheit. Iced saline-soaked towels will be kept in place for a minimum of 5 minutes and replaced at the discretion of the attending obstetrician until the hysterotomy is closed and the uterus is replaced into the patient's abdomen.