Status:
UNKNOWN
Combined Bilateral Uterine Artery Ligation and Bakri Balloon During Cesarean Section
Lead Sponsor:
Aswan University Hospital
Conditions:
Placenta Previa
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
This study will be performed to compare the effectiveness of routine Bakri balloon tamponade and Bilateral Uterine Artery Ligation during cesarean section in patients with placenta previa
Detailed Description
Intraoperative methods to control profuse bleeding during cesarean section in patients with placenta previa include uterine packing, balloon tamponade, uterine compression sutures, arterial ligation, ...
Eligibility Criteria
Inclusion
- women undergoing elective cesarean delivery for complete placenta previa which not respond uterotonic and simple hemostatic maneuvers like placental bed hemostatic sutures
Exclusion
- patients with the high possibility of morbid adherent placenta
- those presented with severe antepartum hemorrhage
- Patients with cardiac, hepatic, renal, or thromboembolic disease;
- patient refuses to consent
Key Trial Info
Start Date :
September 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 31 2022
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT04518150
Start Date
September 1 2020
End Date
October 31 2022
Last Update
September 21 2020
Active Locations (1)
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1
Aswan University Hospital
Aswān, Egypt, 81528