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Intrauterine Misoprostol Versus Intravenous Oxytocin Infusion During Cesarean Delivery

Post Partum Hemorrhage Clinical Trial

Official title:
Intrauterine Misoprostol Versus Intravenous Oxytocin Infusion During Cesarean Delivery to Reduce Intraoperative and Postoperative Blood Loss: A Randomized Clinical Trial.

Clinical Trial Summary

Bleeding is still the major cause of mortality and morbidity in postpartum period. World health organization has reported 585000 deaths for pregnancy each year. Twenty five percent of cases die from post-partum bleeding. Mean amount of blood lost is 500 ml during normal vaginal delivery, 1000 ml in cesarean section, and 3500 ml during cesarean section with emergency hysterectomy

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03148574
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase Phase 3
Start date July 2, 2017
Completion date December 15, 2019
View Details
See also
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