Status:
COMPLETED
Control of Blood Loss During Caesarean Section
Lead Sponsor:
Cairo University
Conditions:
Complications; Cesarean Section
Eligibility:
FEMALE
25-40 years
Phase:
PHASE3
Brief Summary
trial of 3 protocols to determine the best one to control blood loss during caesarean section
Detailed Description
The study population will be divided into 3 groups each containing 200 women: Group (A): 200 patients will receive 5-IU oxytocin bolus over 3 minutes after delivery of the baby. Group (B): 200 patie...
Eligibility Criteria
Inclusion
- Patients booked for elective cesarean section.
- Singleton pregnancies.
- Primigravida or multipara ,first cesarean section or previous .
Exclusion
- Patients with obstetric hemorrhage.
- Uterine laceration.
- Placenta previa.
- Blood dyscrasias.
- Large fibroids.
- Multiple pregnancy.
- Pre-eclampsia.
- Marked maternal anemia.
- Previous history of PPH.
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2014
Estimated Enrollment :
600 Patients enrolled
Trial Details
Trial ID
NCT01412073
Start Date
September 1 2011
End Date
October 1 2014
Last Update
October 7 2014
Active Locations (1)
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1
faculty of medicine , Cairo University
Cairo, Cairo Governorate, Egypt, 12211