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Carbetocin Versus Oxytocin for Prophylaxis Against Atonic Primary Post-partum Hemorrhage

High Risk Pregnancy Clinical Trial

Official title:
Carbetocin Versus Oxytocin for Prophylaxis Against Atonic Primary Post-partum Hemorrhage in High-risk Patients in Sohag University Hospital: A Randomized Controlled Clinical Trial

Clinical Trial Summary

Comparison between Carbetocin and Oxytocin as prophylaxis against Primary Postpartum Hemorrhage.

Clinical Trial Description

Patients will be allocated randomly by simple randomization into either 1- the control group which will be given 10 IU oxytocin intravenously, OR 2- the treatment group which will be given 100 micrograms of carbetocin intravenously. The trial will be conducted on patients with high risk of developing atonic primary postpartum hemorrhage. The trial will be single blinded. All patients fulfilling the inclusion criteria undergoing elective Caesarean section will be approached by the treating physician and will be asked to participate in the study. An informed written consent will be taken from each patient. The data collected will include base line characteristics such as age, parity, body mass index, the risk for Postpartum hemorrhage in each patient, amount of blood loss, blood units given, complete blood picture (pre and post operative) and coagulation profile. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05479357
Study type Interventional
Source Sohag University
Contact Eman M Sabry, MBBCh
Phone +201012733125
Email emanmahmoud@med.sohag.edu.eg
Status Not yet recruiting
Phase N/A
Start date July 28, 2022
Completion date December 30, 2022
View Details
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